Library preparation of tagged nucleic acid

ABSTRACT

A method of preparing a library of tagged nucleic acid fragments including contacting a population of cells directly with a lysis reagent having one or more protease to generate a cell lysate; inactivating the protease to generate an inactivated cell lysate, and applying a transposase and a transposon end composition containing a transferred strand to the inactivated cell lysate under conditions wherein the target nucleic acid and the transposon end composition undergo a transposition reaction.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation application of U.S. patentapplication Ser. No. 14/749,562, filed Jun. 24, 2015, which claimspriority to U.S. provisional application No. 62/017,786, filed Jun. 26,2014; and U.S. provisional application No. 62/027,198, filed Jul. 21,2014, each of which is incorporated herein by reference in its entirety.

SEQUENCE LISTING

This application contains a Sequence Listing electronically submitted tothe United States Patent and Trademark Office via EFS-Web on Jun. 28,2018, as an ASCII text file entitled “1246A_ST25.txt,” having a size of775 bytes and created on Jun. 27, 2018. Due to the electronic filing ofthe Sequence Listing, the electronically submitted Sequence Listingserves as both the paper copy required by 37 CFR § 1.821(c) and the CRFrequired by § 1.821(e). The information contained in the SequenceListing is herein incorporated by reference in its entirety.

FIELD

The present disclosure relates generally to methods for preparing alibrary of nucleic acid fragments, and more specifically to methods forpreparing a library of nucleic acid fragments in a single tube usingproteases for a variety of applications including, e.g., next generationDNA sequencing.

BACKGROUND

There are a variety of methods and applications for which it isdesirable to generate a library of fragmented and tagged nucleic acid,e.g., for use as templates in DNA sequencing and/or for analysis of copynumber variation.

Recently developed “next generation” DNA sequencing technologies, suchas those developed by Illumina, Inc. (San Diego, Calif.), enablegenerating sequence data from up to millions of sequencing templates ina single sequence run using a massively parallel or multiplex format.This massively parallel nature of “next generation” sequencing requiresgenerating libraries of nucleic acid fragments containing a collectionor population of nucleic acid fragments from target nucleic acid sample,e.g., a genome DNA. More importantly, it requires that the combinationof these nucleic acid fragments exhibits sequences that arequalitatively and/or quantitative representative of the sequence fromthe target nucleic acid sample. When nucleic acid sample is from cells,current methods for generating a library of nucleic acid fragmentstypically require a separate step for isolating target nucleic acid fromcells, prior to nucleic acid fragmentation. This nucleic acid extractionstep is usually wasteful of target nucleic acid sample, and usuallyrenders the nucleic acid prepared unable to qualitatively represent thetarget nucleic acid from the sample. This becomes a particularly seriousproblem when the amount of sample is limited or difficult to obtain. Tosolve this problem, some current methods use nucleic acid amplificationprior to fragmentation. However, amplification cannot ensure therepresentativeness of the target nucleic acid since the target nucleicacid is still partially lost during extraction prior to amplification.

Thus, there exists a need for new methods that enable rapid andefficient preparation of nucleic acid fragment library. The presentdisclosure addresses this need by providing methods for preparing alibrary of nucleic acid fragments in a single reaction mixture, e.g., ina single tube, using proteases. Related advantages are provided as well.

SUMMARY

In one aspect, provided herein is a method of preparing a library oftagged nucleic acid fragments including (a) contacting a population ofcells directly with a lysis reagent to generate a cell lysate, whereinthe lysis reagent has one or more proteases, and wherein the cell lysatecontains a target nucleic acid; (b) inactivating the one or moreproteases to form an inactivated cell lysate, and (c) directly applyingat least one transposase and at least one transposon end compositioncontaining a transferred strand to the inactivated cell lysate underconditions where the target nucleic acid and the transposon endcomposition undergo a transposition reaction to generate a mixture,wherein (i) the target nucleic acid is fragmented to generate aplurality of target nucleic acid fragments, and (ii) the transferredstrand of the transposon end composition is joined to 5′ ends of each ofa plurality of the target nucleic acid fragments to generate a pluralityof 5′ tagged target nucleic acid fragments.

In some embodiments, steps (a), (b), and (c) provided herein areperformed in a single reaction mixture, e.g., in a tube. In someembodiments, the population of cells is a minimal population of cells.In some embodiments, the minimal population of cells contains one, two,three, four, or five cells.

In some embodiments, the one or more proteases are selected from a groupconsisting of serine proteases, threonine proteases, cysteine proteases,aspartate proteases, glutamic acid proteases, and metalloproteases. Insome embodiments, the one or more proteases are subtilisins and variantsthereof. In some embodiments, the concentration of one or more proteasesin the cell lysate is 0.1 mg/ml to 10 mg/ml. In some embodiments, theconcentration of the one or more proteases in the cell lysate is 0.1mg/ml to 2.5 mg/ml. In some embodiments, the concentration of the one ormore proteases in the cell lysate is 0.5 mg/ml. In some embodiments, theconcentration of the one or more proteases in the cell lysate is 4.5mAU/ml to 500 mAU/ml. In some embodiments, the concentration of the oneor more proteases in the cell lysate is 22.5 mAU/ml.

In some embodiments, the population of cells are contacted with thelysis reagent at pH 7.0 to pH 10.0 in step (a). In some embodiments, thepopulation of cells are contacted with the lysis reagent at pH 7.0 to pH9.0.

In some embodiments, the one or more proteases are inactivated byincreasing temperature in step (b). In some embodiments, the one or moreproteases are inactivated by increasing temperature to 50° C.-80° C. Insome embodiments, the one or more proteases are inactivated byincreasing temperature to 70° C. In some embodiments, the one or moreproteases are inactivated by adding one or more inhibitors of the one ormore proteases.

In some embodiments, the lysis reagent includes one or more detergents.In some embodiments, the one or more detergents are nonionic detergents.In some embodiments, the one or more detergents include TRITON.

In some embodiments, the target nucleic acid is a double-stranded DNA,and wherein the target nucleic acid remains the double-stranded DNAprior to applying a trasposease and a trasposon end composition in step(c). In some embodiments, the target nucleic acid is genomic DNA. Insome embodiments, the target nucleic acid contains chromosomal DNA or afragment thereof. In some embodiments, the target nucleic acid includesa genome or a partial genome.

In some embodiments, the at least one transposase is a Tn5 transposase.In some embodiments, the at least one transposon end compositionincludes Tn5 transposon end.

In some embodiments, the transferred strand includes tag domainscontaining one or more of a restriction site domain, a capture tagdomain, a sequencing tag domain, an amplification tag domain, adetection tag domain, and an address tag domain.

In some embodiments, the method provided herein further includes (d)incubating the mixture from step (c) directly with at least one nucleicacid modifying enzyme under conditions wherein a 3′ tag is joined to the5′ tagged target nucleic acid fragments to generate a plurality ofdi-tagged target nucleic acid fragments. In some embodiments, steps (a),(b), (c), and (d) are performed in a single reaction tube.

In some embodiments, the nucleic acid modifying enzyme is a polymeraseand wherein said 3′ tag is formed by extension of the 3′ end of the 5′tagged target nucleic acid fragment. In some embodiments, the nucleicacid modifying enzyme is a ligase and wherein the 3′ tag is formed byligation of an oligonucleotide to the 3′ end of the 5′ tagged targetnucleic acid fragment.

In some embodiments, the method provided herein further includes (e)amplifying one or more di-tagged target nucleic acid fragments togenerate a library of tagged nucleic acid fragments with additionalsequence at 5′ end and/or 3′ end of the di-tagged nucleic acidfragments. In some embodiments, steps (a), (b), (c), (d), and (e) areperformed in a single reaction tube.

In some embodiments, the amplifying includes use of one or more of apolymerase chain reaction (PCR), a strand-displacement amplificationreaction, a rolling circle amplification reaction, a ligase chainreaction, a transcription-mediated amplification reaction, or aloop-mediated amplification reaction. In some embodiments, theamplifying includes a PCR using a single primer that is complementary tothe 3′ tag of the di-tagged target DNA fragments. In some embodiments,the amplifying includes a PCR using a first and a second primer, whereinat least a 3′ end portion of the first primer is complementary to atleast a portion of the 3′ tag of the di-tagged target nucleic acidfragments, and wherein at least a 3′ end portion of the second primerexhibits the sequence of at least a portion of the 5′ tag of thedi-tagged target nucleic acid fragments. In some embodiments, a 5′ endportion of the first primer is non-complementary to the 3′ tag of thedi-tagged target nucleic acid fragments, and a 5′ end portion of thesecond primer does not exhibit the sequence of at least a portion of the5′ tag of the di-tagged target nucleic acid fragments. In someembodiments, the first primer includes a first universal sequence,and/or wherein the second primer includes a second universal sequence.

In some embodiments, the method provided herein further includessequencing the tagged nucleic acid fragments. In some embodiments, thesequencing of the tagged nucleic acid fragments includes use of one ormore of sequencing by synthesis, bridge PCR, chain terminationsequencing, sequencing by hybridization, nanopore sequencing, andsequencing by ligation. In some embodiments, the sequencing of thetagged nucleic acid fragments includes use of next generationsequencing.

In some embodiments, the method provided herein further includesanalyzing copy number variation. In some embodiments, the methodprovided herein further includes analyzing single nucleotide variation.

In another aspect, the present disclosure provides a kit for preparing alibrary of tagged nucleic acid fragments including (a) a lysis reagenthaving one or more proteases, and (b) a transposition reactioncomposition having at least one transposase and at least one transposonend composition containing a transferred strand.

In some embodiments, the one or more proteases are selected from a groupconsisting of serine proteases, threonine proteases, cysteine proteases,aspartate proteases, glutamic acid proteases, and metalloproteases. Insome embodiments, the one or more proteases are subtilisins and variantsthereof. In some embodiments, the lysis agent includes one or moredetergents. In some embodiments, the one or more detergents includeTRITON.

In some embodiments, the at least one transposon end composition includea tag domain and a 3′ portion comprising the transferred strand. In someembodiments, the tag domain includes one or more of a restriction sitedomain, a capture tag domain, a sequencing tag domain, an amplificationtag domain, a detection tag domain, and an address tag domain. In someembodiments, the transposition reaction composition includes two or moretransposon end compositions, each of the two or more transposon endcompositions includes a transferred strand that differs by at least onenucleotide. In some embodiments, the transposase is a Tn5 transposase.In some embodiments, the transposon end composition includes a Tn5transposon end.

In some embodiments, the kit provided herein further includes apolymerase. In some embodiments, the kit provided herein furtherincludes a ligase.

In some embodiments, the kit provided herein further includes a reagentfor an amplification reaction. In some embodiments, the reagent for theamplification reaction is a reagent for PCR. In some embodiments, thereagent for the amplification reaction includes at least one primer. Insome embodiments, the at least one primer includes a 3′ portion thatexhibits the sequence of at least a portion of the transferred strand.In some embodiments, the at least one primer includes a 5′ portion thatcontains a universal sequence.

In some embodiments, the kit provided herein further includes a sizeselection reagent. In some embodiments, the size selection reagentincludes AMPURE XP beads. In some embodiments, the kit provided hereinfurther includes a library normalization reagent.

In some embodiments, the kit provided herein further includes anapparatus having a solid surface. In some embodiments, the apparatus isa flow cell apparatus. In some embodiments, the solid surface includes apatterned surface suitable for immobilization of a molecule in anordered pattern.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a histogram showing the percentage of unique mapped read in asequencing using 0 mg/ml, 0.1 mg/ml, 0.5 mg/ml, or 2.5 mg/ml proteasestreated whole cells or nuclei.

FIG. 2 show histograms of copy number analysis results using bulk DNA,single cell treated with sufficient protease activity, and single celltreated with insufficient protease activity.

FIG. 3A shows histograms of copy number analysis results in a singlecell treated with 0.5 mg/ml active protease, 2 mg/ml active protease, or2 mg/ml pre-heat inactivated protease. FIG. 3B shows a histogram ofpercentage of unique mapped read in a sequencing of a single celltreated with 0.5 mg/ml active protease, 1 mg/ml active protease, 2 mg/mlprotease under reaction temperature, or 2 mg/ml pre-heat inactivatedprotease, and a control sample without cells. FIG. 3C shows a histogramof read count differences between neighboring bins (Inter Quartile Rangeof read count difference between neighboring bins) in a sequencing of asingle cell treated with active 0.5 mg/ml protease, 1 mg/ml activeprotease, 2 mg/ml active protease, or 2 mg/ml pre-heat inactivatedprotease, and a control sample without cells.

FIG. 4A is a histogram showing relative activity of protease under pH7.0, pH 7.5, pH 8.0, pH 8.5, pH 9.0, or pH 10.0. FIG. 4B shows ahistogram of percentage of unique mapped reads in a sequencingexperiment of a single cell treated with protease under pH 7.0, pH 8.0,pH 9.0, or pH 10.0. FIG. 4C shows a histogram of read count differencesbetween neighboring bins (Inter Quartile Range of read count differencebetween neighboring bins) in a sequencing experiment of a single celltreated with protease under pH 7.0, pH 8.0, pH 9.0, or pH 10.0.

FIG. 5A is a histogram showing relative protease activity pre-heated atroom temperature, 50° C., 60° C., or 70° C. FIG. 5B shows a histogram ofpercentage of unique mapped reads in a sequencing experiment of a singlecell, three cells, or 15 pg genomic DNA, treated with proteasepre-heated at room temperature, 50° C., 60° C., or 70° C. FIG. 5C showsa histogram of read count differences between neighboring bins (InterQuartile Range of read count difference between neighboring bin) in asequencing experiment of a single cell, three cells, or 15 pg genomicDNA, treated with protease pre-heated at room temperature, 50° C., 60°C., or 70° C.

FIG. 6A shows insert size of a library generated with treatment of 1 μlTn5 or 2 μl Tn5. FIG. 6B shows insert size of a library generated withtreatment of 1 μl Tn5 or 2 μl Tn5.

FIG. 6C shows diversity of libraries generated with treatment of 1 μlTn5 or 2 μl Tn5.

FIG. 7 shows histograms of counts and copy number analysis results in asequencing experiment of a single cell according to the method providedherein using PCR with 16 cycles, 18 cycles, or 20 cycles.

FIG. 8A shows read distribution of three single-cell sequencingexperiments.

FIG. 8B shows read distribution of single-cell sequencing, three-cellsequencing, or five-cell sequencing. FIG. 8C shows histograms of averagelibrary diversity and estimated genome coverage using a single cell,three cells or five cells. FIG. 8D shows overall protocol success rate.

FIG. 9A shows copy number analysis using REPLIg Single Cell (MDA) withNexteral XT library preparation. FIG. 9B shows copy number analysisusing SurePlex with Nexteral XT library preparation. FIG. 9C shows copynumber analysis using Nextera Single Cell provided herein.

FIG. 10A shows copy number analysis data of chromosome 18 using threerelicates of a single GM50121 cell. FIG. 10B shows count number datausing three replicates of a single GM20916 cell. FIG. 10C shows copynumber analysis data of chromosomes 15, X, and 10 using three replicatesof a single GM20916 cell. FIG. 10D shows copy number analysis data ofchromosomes 1 and 11 using three replicates of a single GM10239 cell.

DETAILED DESCRIPTION

The present disclosure relates generally to methods for preparing alibrary of nucleic acid fragments, and more specifically to methods forpreparing a library of nucleic acid fragments in a single reactionmixture, e.g., a single tube, using proteases for a variety ofapplications including, e.g., next generation sequencing.

Definitions

As used herein, the terms “includes,” “including,” “includes,”“including,” “contains,” “containing,” “have,” “having,” and anyvariations thereof, are intended to cover a non-exclusive inclusion,such that a process, method, product-by-process, or composition ofmatter that includes, includes, or contains an element or list ofelements does not include only those elements but can include otherelements not expressly listed or inherent to such process, method,product-by-process, or composition of matter.

As used herein, the terms “a” and “an” and “the” and similar referentsin the context of describing the invention (especially in the context ofthe following claims) are to be construed to cover both the singular andthe plural, unless otherwise indicated herein or clearly contradicted bycontext.

As used herein, the term “about” or “approximately” means within 5% of agiven value or range.

As used herein, the term “a minimal population of cells” means apopulation of cells that contains an amount of DNA copies that is belownucleic acid sequencing capabilities absent a separation step such asDNA extraction prior to tagmentation. Exemplary separation steps includeextracting DNA content from a cell lysate, and/or DNA amplification. Aminimal population of cells can include one, two, three, four, or fivecells. A minimal population of cells can be a single cell. “Nucleic acidsequencing capabilities,” as used herein, means sequencing capabilitythat can produce clean copy number variation data of a genome.

As used herein, the term “nucleic acid” means single-stranded anddouble-stranded polymers of nucleotide monomers, including2′-deoxyribonucleotides (DNA) and ribonucleotides (RNA) linked byinternucleotide phosphodiester bond linkages, or internucleotideanalogs, and associated counter ions, e.g, H+, NH4+, trialkylammonium,tetraalkylammonium, Mg2+, Na+ and the like. A nucleic acid includespolynucleotide and oligonucleotide. A nucleic acid may be composedentirely of deoxyribonucleotides, entirely of ribonucleotides, orchimeric mixtures thereof. The nucleotide monomer units may include anyof the nucleotides described herein, including, but not limited to,naturally occurring nucleotides and nucleotides analogs. Nucleic acidtypically ranges in size from a few monomeric units, e.g, 5-40, toseveral thousands of monomeric nucleotide units. Nucleic acids include,but are not limited to, genomic DNA, cDNA, hnRNA, mRNA, rRNA, tRNA,fragmented nucleic acid, nucleic acid obtained from sub-cellularorganelles such as mitochondria or chloroplasts, and nucleic acidobtained from microorganisms or DNA or RNA viruses that may be presenton or in a biological sample.

As used herein, the term “target nucleic acid” is intended to mean anucleic acid that is the object of an analysis or action. The analysisor action includes subjecting the nucleic acid to copying,amplification, sequencing and/or other procedure for nucleic acidinterrogation. A target nucleic acid can include nucleotide sequencesadditional to the target sequence to be analyzed. For example, a targetnucleic acid can include one or more adapters, including an adapter thatfunctions as a primer binding site, that flank(s) a target nucleic acidsequence that is to be analyzed. A target nucleic acid hybridized to acapture oligonucleotide or capture primer can contain nucleotides thatextend beyond the 5′ or 3′ end of the capture oligonucleotide in such away that not all of the target nucleic acid is amenable to extension.

As used herein, the terms “isolate” and “purify” as used herein, referto the reduction in the amount of at least one contaminant (such asprotein and/or nucleic acid sequence) from a sample or from a sourcefrom which the material is isolated or purified.

As used herein, the term “size selection” means a procedure during whicha sub-population of nucleic acid fragments, majority of which have anumber of nucleotides falling in a defined range, is selected from apopulation of nucleic acid fragments, and thus the percentage of nucleicacid fragments having a number of nucleotides falling in the definedrange increases.

As used herein, the term “protease” refers to a protein, polypeptide orpeptide exhibiting the ability to hydrolyze polypeptides or substrateshaving a polypeptide portion. The protease(s) provided in the presentmethods can be a single protease possessing broad specificity. Thepresent methods can use a mixture of various proteases. The proteasesprovided herein can be heat-labile and thus can be inactivated by heat.In certain embodiments, the proteases provided herein can be inactivatedat a temperature above about 25° C., 30° C., 35° C., 40° C., 45° C., 50°C., 55° C., 60° C., 65° C., 70° C., 75° C., 80° C. or above about 85° C.The proteases provided herein can digest chromatin proteins and otherDNA-binding proteins to release naked genomic DNA, and can also digestendogenous DNase to protect DNA from degradation. The proteases providedherein include, but not limited to, serine proteases, threonineproteases, cysteine proteases, aspartate proteases, glutamic acidproteases, and metalloproteases. Typically, aspartic, glutamic andmetallo proteases activate a water molecule which performs anucleophilic attack on the peptide bond to hydrolyze it. Serine,threonine and cysteine proteases typically use a nucleophilic residue toperform a nucleophilic attack to covalently link the protease to thesubstrate protein, releasing the first half of the product. Thiscovalent acyl-enzyme intermediate is then hydrolyzed by activated waterto complete catalysis by releasing the second half of the product andregenerating the free enzyme. Exemplary protease used herein includes aserine protease isolated from a recombinant Bacillus strain. Exemplaryproteases used herein include subtilisin and variants thereof, includingsubtilisin Carlsberg, ALCALASE, and subtilisin S41. Subtilisins andvariants thereof are known to those of skill in the art and include, forexample ALCALASE, ALCALASE 0.6L, ALCALASE 2.5L, ALK-enzyme,bacillopeptidase A, bacillopeptidase B, Bacillus subtilis alkalineproteinase bioprase, bioprase AL 15, bioprase APL 30, colistinase,subtilisin J, subtilisin S41, subtilisin Sendai, subtilisin GX,subtilisin E, subtilisin BL, GENENASE I, ESPERASE, MAXATASE, thermoasePC 10, protease XXVII, thermoase, SUPERASE, subtilisin Carlsbergsubtilisin DY, subtilopeptidase, SP 266, SAVINASE 8.0L, SAVINASE 4.0T,KAZUSASE, protease VIII, OPTICLEAN, protin A 3L, SAVINASE, SAVINASE16.0L, SAVINASE 32.0L EX, orientase 10B, protease S, serineendopeptidase. In particular embodiments of the methods and compositionspresented herein, a heat-labile protease such as subtilisin andheat-labile variants of subtilisin can be used, as represented by theexemplary disclosure of Davail et al., 1994, J. Biol. Chem.,26:17448-17453, which is incorporated herein by reference in itsentirety.

As used herein, the term “protease inhibitor” refers to a substance,e.g., a compound, capable of at least partially reducing the ability ofa protease to hydrolyze peptides.

As used herein, the term “ligase” refers to a nucleic acid modifyingenzyme that catalyzes intra- and intermolecular formation ofphosphodiester bonds between 5′-phosphate and 3′-hydroxyl termini ofnucleic acid strands. Ligases include, e.g., template-independentligases, such as CIRCLIGASE™ ssDNA ligase, that can join ends ofsingle-stranded RNA and DNA, and template-dependent, that seal nicks indouble-stranded DNA. As used herein, “template-dependent ligase” means aDNA ligase that catalyzes intra- and intermolecular formation ofphosphodiester bonds between 5′-phosphate and 3′-hydroxyl termini of DNAstrands that are adjacent to each other when annealed to a complementarypolynucleotide. The polynucleotide to which both of the DNA ends to beligated anneal adjacently is referred to herein as a “ligation template”and the ligation is referred to as “template-dependent ligation.” Theligation template can be a complementary DNA sequence in genomic orother DNA in a biological sample, or the ligation template can be a“bridging oligodeoxyribonucleotide” or “ligation splintoligodeoxyribonucleotide” (or “ligation splint”) that is synthesizedand/or provided specifically for use in a particular assay or method.Examples template-dependent DNA ligases include NAD-type DNA ligasessuch as E. coli DNA ligase, Tth DNA ligase, TfI DNA ligase, andAMPLIGASE® DNA ligase (EPICENTRE Biotechnologies, Madison, Wis., USA),which catalyze intramolecular ligation of ssDNA molecules only in thepresence of a ligation template, and ATP-type DNA ligases, such as T4DNA ligase or FASTLINK™ DNA ligase (EPICENTRE Biotechnologies).

As used herein, the term “tagmentation” refers to the modification ofDNA by a transposome complex comprising transposase enzyme complexedwith adaptors comprising transposon end sequence. Tagmentation resultsin the simultaneous fragmentation of the DNA and ligation of theadaptors to the 5′ ends of both strands of duplex fragments. Additionalsequences can be added to the ends of the adapted fragments, for exampleby PCR, ligation, or any other suitable methodology known to those ofskill in the art. As used herein, the term “transposome complex” refersto a transposase enzyme non-covalently bound to a double strandednucleic acid. For example, the complex can be a transposase enzymepreincubated with double-stranded transposon DNA under conditions thatsupport non-covalent complex formation. Double-stranded transposon DNAcan include, without limitation, Tn5 DNA, a portion of Tn5 DNA, atransposon end composition, a mixture of transposon end compositions orother double-stranded DNAs capable of interacting with a transposasesuch as the hyperactive Tn5 transposase.

As used herein, the term “transposition reaction” refers to a reactionwherein one or more transposons are inserted into target nucleic acids,e.g., at random sites or almost random sites. Essential components in atransposition reaction are a transposase and DNA oligonucleotides thatexhibit the nucleotide sequences of a transposon, including thetransferred transposon sequence and its complement (the non-transferredtransposon end sequence) as well as other components needed to form afunctional transposition or transposome complex. The DNAoligonucleotides can further include additional sequences (e.g., adaptoror primer sequences) as needed or desired. In some embodiments, themethod provided herein is exemplified by employing a transpositioncomplex formed by a hyperactive Tn5 transposase and a Tn5-typetransposon end (Goryshin and Reznikoff, 1998, J. Biol. Chem., 273: 7367)or by a MuA transposase and a Mu transposon end comprising R1 and R2 endsequences (Mizuuchi, 1983, Cell, 35: 785; Savilahti et al., 1995, EMBOJ., 14: 4893). However, any transposition system that is capable ofinserting a transposon end in a random or in an almost random mannerwith sufficient efficiency to 5′-tag and fragment a target DNA for itsintended purpose can be used in the present invention. Examples oftransposition systems known in the art which can be used for the presentmethods include but are not limited to Staphylococcus aureus Tn552(Colegio et al., 2001, J Bacterid., 183: 2384-8; Kirby et al., 2002, MOIMicrobiol, 43: 173-86), TyI (Devine and Boeke, 1994, Nucleic Acids Res.,22: 3765-72 and International Patent Application No. WO 95/23875),Transposon Tn7 (Craig, 1996, Science. 271: 1512; Craig, 1996, Review in:Curr Top Microbiol Immunol, 204: 27-48), TnIO and ISIO (Kleckner et al.,1996, Curr Top Microbiol Immunol, 204: 49-82), Mariner transposase(Lampe et al., 1996, EMBO J., 15: 5470-9), Tci (Plasterk, 1996, Curr TopMicrobiol Immunol, 204: 125-43), P Element (Gloor, 2004, Methods MolBiol, 260: 97-114), TnJ (Ichikawa and Ohtsubo, 1990, J Biol Chem. 265:18829-32), bacterial insertion sequences (Ohtsubo and Sekine, 1996,Curr. Top. Microbiol. Immunol. 204:1-26), retroviruses (Brown et al.,1989, Proc Natl Acad Sci USA, 86: 2525-9), and retrotransposon of yeast(Boeke and Corces, 1989, Annu Rev Microbiol. 43: 403-34). The method forinserting a transposon end into a target sequence can be carried out invitro using any suitable transposon system for which a suitable in vitrotransposition system is available or that can be developed based onknowledge in the art. In general, a suitable in vitro transpositionsystem for use in the methods provided herein requires, at a minimum, atransposase enzyme of sufficient purity, sufficient concentration, andsufficient in vitro transposition activity and a transposon end withwhich the transposase forms a functional complex with the respectivetransposase that is capable of catalyzing the transposition reaction.Suitable transposase transposon end sequences that can be used in theinvention include but are not limited to wild-type, derivative or mutanttransposon end sequences that form a complex with a transposase chosenfrom among a wild-type, derivative or mutant form of the transposase.

As used herein, the term “transposase” refers to an enzyme that iscapable of forming a functional complex with a transposon end-containingcomposition (e.g., transposons, transposon ends, transposon endcompositions) and catalyzing insertion or transposition of thetransposon end-containing composition into the double-stranded targetnucleic acid with which it is incubated, for example, in an in vitrotransposition reaction. A transposase as presented herein can alsoinclude integrases from retrotransposons and retroviruses. Transposases,transposomes and transposome complexes are generally known to those ofskill in the art, as exemplified by the disclosure of US 2010/0120098,the content of which is incorporated herein by reference in itsentirety. Although many embodiments described herein refer to Tn5transposase and/or hyperactive Tn5 transposase, it will be appreciatedthat any transposition system that is capable of inserting a transposonend with sufficient efficiency to 5′-tag and fragment a target nucleicacid for its intended purpose can be used in the present invention. Inparticular embodiments, a transposition system is capable of insertingthe transposon end in a random or in an almost random manner to 5′-tagand fragment the target nucleic acid.

As used herein, the term “transposon end” means a double-stranded DNAthat exhibits only the nucleotide sequences (the “transposon endsequences”) that are necessary to form the complex with the transposaseor integrase enzyme that is functional in an in vitro transpositionreaction. A transposon end forms a “complex” or a “synaptic complex” ora “transposome complex” or a “transposome composition with a transposaseor integrase that recognizes and binds to the transposon end, and whichcomplex is capable of inserting or transposing the transposon end intotarget DNA with which it is incubated in an in vitro transpositionreaction. A transposon end exhibits two complementary sequencesconsisting of a “transferred strand” and a “non transferred strand.” Forexample, one transposon end that forms a complex with a hyperactive Tn5transposase (e.g., EZ-Tn5™ Transposase, EPICENTRE Biotechnologies,Madison, Wis., USA) that is active in an in vitro transposition reactioncomprises a transferred strand that exhibits a “transferred transposonend sequence” as follows: 5′ AGATGTGTATAAGAGACAG 3′ (SEQ ID NO:1), and anon-transferred strand that exhibits a “non-transferred transposon endsequence” as follows: 5′ CTGTCT CTTATACACATCT 3′ (SEQ ID NO:2). The3′-end of a transferred strand is joined or transferred to targetnucleic acid in an in vitro transposition reaction. The non-transferredstrand, which exhibits a transposon end sequence that is complementaryto the transferred transposon end sequence, is not joined or transferredto the target nucleic acid in an in vitro transposition reaction.

As used herein, the term “transposon end composition” refers to acomposition comprising a transposon end (the minimum double-stranded DNAsegment that is capable of acting with a transposase to undergo atransposition reaction), optionally plus additional sequence orsequences. 5′-of the transferred transposon end sequence and/or 3′-ofthe non-transferred transposon end sequence. For example, a transposonend attached to a tag is a “transposon end composition.”

As used herein, the term “transferred strand” refers to the transferredportion of both “transposon ends” and “transposon end compositions”(regardless of whether the transposon end is attached to a tag or othermoiety). Similarly, the term “non-transferred strand” refers to thenon-transferred portion of both “transposon ends” and “transposon endcompositions.”

As used herein, the term “tag” refers to a non-target nucleic acidcomponent, generally DNA, that provides a means of addressing a nucleicacid fragment to which it is joined. For example, in some embodiments, atag comprises a nucleotide sequence that permits identification,recognition, and/or molecular or biochemical manipulation of the DNA towhich the tag is attached (e.g., by providing a site for annealing anoligonucleotide, such as a primer for extension by a DNA polymerase, oran oligonucleotide for capture or for a ligation reaction). The processof joining the tag to the nucleic acid molecule is sometimes referred toherein as “tagging” and the nucleic acid that undergoes tagging or thatcontains a tag is referred to as “tagged” (e.g., “tagged DNA”).

As used herein, the term “tag domain” refers to a portion or domain of atag that exhibits a sequence for a desired intended purpose orapplication. One tag domain is the “transposon end domain,” which tagdomain exhibits the transferred transposon end sequence. In someembodiments, the transferred strand also exhibits one or more othernucleotide sequences 5′-of the transferred transposon end sequence, thetag also has one or more other “tag domains” in the 5′-portion, each ofwhich tag domains is provided for any desired purpose. For example, someembodiments contain a transposon end composition that includes a tagdomain selected from among one or more of a restriction site tag domain,a capture tag domain, a sequencing tag domain, an amplification tagdomain, a detection tag domain, an address tag domain, and atranscription promoter domain.

As used herein, the term “restriction site domain” refers to a tagdomain that exhibits a sequence for the purpose of facilitating cleavageusing a restriction endonuclease. For example, the restriction sitedomain can be used to generate di-tagged linear ssDNA fragments. Therestriction site domain can also be used to generate a compatibledouble-stranded 5′-end in the tag domain so that this end can be ligatedto another DNA molecule using a template-dependent DNA ligase.

As used herein, the term “capture tag domain” refers to a tag domainthat exhibits a sequence for the purpose of facilitating capture of thenucleic acid fragment to which the tag domain is joined (e.g., toprovide an annealing site or an affinity tag for a capture of thedi-tagged linear ssDNA fragments on a bead or other surface, e.g.,wherein the annealing site of the tag domain sequence permits capture byannealing to a specific sequence which is on a surface, such as a probeon a bead or on a microchip or microarray or on a sequencing bead). Insome embodiments, the capture tag domain comprises a 5′-portion of thetransferred strand that is joined to a chemical group or moiety thatincludes an affinity binding molecule (e.g., biotin, streptavidin, anantigen, or an antibody that binds the antigen, that permits capture ofthe di-tagged linear ssDNA fragments on a surface to which a secondaffinity binding molecule is attached that forms a specific binding pairwith the first affinity binding molecule).

As used herein, the term “sequencing tag domain” refers to a tag domainthat exhibits a sequence for the purposes of facilitating sequencing ofthe nucleic acid fragment to which the tag is joined (e.g., to provide apriming site for sequencing by synthesis, or to provide annealing sitesfor sequencing by ligation, or to provide annealing sites for sequencingby hybridization).

As used herein, the term “amplification tag domain” refers to a tagdomain that exhibits a sequence for the purpose of facilitatingamplification of a nucleic acid to which said tag is appended. Forexample, in some embodiments, the amplification tag domain provides apriming site for a nucleic acid amplification reaction using a DNApolymerase (e.g., a PCR amplification reaction or a strand-displacementamplification reaction, or a rolling circle amplification reaction), ora ligation template for ligation of probes using a template-dependentligase in a nucleic acid amplification reaction (e.g., a ligation chainreaction).

As used herein, the term “detection tag domain” refers to a tag domainthat exhibits a sequence or a detectable chemical or biochemical moietyfor the purpose of facilitating detection of the tagged nucleic acidfragments (e.g., a visible, fluorescent, chemiluminescent, or otherdetectable dye; an enzyme that is detectable in the presence of asubstrate, e.g., an alkaline phosphatase with NBT plus BCIP or aperoxidase with a suitable substrate; a detectable protein, e.g., agreen fluorescent protein; and an affinity-binding molecule that isbound to a detectable moiety or that can form an affinity binding pairor a specific binding pair with another detectable affinity-bindingmolecule; or any of the many other detectable molecules or systems knownin the art).

As used herein, the term “address tag domain” means a tag domain thatexhibits a sequence that permits identification of a specific sample(e.g., wherein the transferred strand has a different address tag domainthat exhibits a different sequence for each sample).

As used herein, the terms “amplify” or “amplified” “amplifying” as usedin reference to a nucleic acid or nucleic acid reactions, refer to invitro methods of making copies of a particular nucleic acid, such as atarget nucleic acid, or a tagged nucleic acid. Numerous methods ofamplifying nucleic acids are known in the art, and amplificationreactions include, but not limited to, polymerase chain reactions,ligase chain reactions, strand displacement amplification reactions,rolling circle amplification reactions. The nucleic acid that isamplified can be DNA. The products resulting from amplification of anucleic acid molecule or molecules (“amplification products”), whetherthe starting nucleic acid is DNA, RNA or both, can be either DNA or RNA,or a mixture of both DNA and RNA nucleosides or nucleotides, or they caninclude modified DNA or RNA nucleosides or nucleotides. A “copy” doesnot necessarily mean perfect sequence complementarily or identity to thetarget sequence. For example, copies can include nucleotide analogs suchas deoxyinosine or deoxyuridine, intentional sequence alterations (suchas sequence alterations introduced through a primer containing asequence that is hybridizable, but not complementary, to the targetsequence), and/or sequence errors that occur during amplification.

A as used herein, the term a “library of tagged nucleic acid fragments”refers to a collection or population of tagged nucleic acid fragments(e.g., di-tagged nucleic acid fragments) generated from a resource,e.g., whole genome, wherein the combination of the tagged nucleic acidfragments in the collection or population exhibits sequences that arequalitatively and/or quantitatively representative of the sequence ofthe resource from which the tagged nucleic acid fragments weregenerated, e.g., whole genome. It is possible that a library of taggednucleic acid fragments does not contain a tagged nucleic fragmentrepresenting every sequence which is exhibited by the resource.

As used herein, the term “nucleic acid modifying enzyme” refers to anyenzyme that acts upon nucleic acid, e.g., DNA, to effect a modification,e.g., cleavage, ligation, polymerization, phosphorylation, etc. Nucleicacid modifying enzymes include, e.g., polymerases, nucleases,transferases, ligases, phosphorylases, phosphatases, methylases,transosases, etc. “DNA modifying enzymes” include any enzymes that acton DNA, including enzymes that also act on other substrates, such asRNA.

As used herein, the term “DNA polymerase” refers to a modifying enzymethat catalyzes the polymerization of deoxyribonucleotides into a DNAstrand. DNA polymerases include “template-dependent DNA polymerases,”which require a template nucleic acid to determine the order in whichdeoxyribonucleotides are added in the polymer, or they may be“template-independent” such that they catalyze polymerization withoutreference to a template sequence. In addition to synthesizing DNApolymers, DNA polymerases may comprise other features or activities. Forexample, a DNA polymerase may be characterizes as having or lacking 5′to 3′ exonuclease activity (also referred to a 5′ exonuclease or 5′nuclease activity), 3′ to 5′ exonuclease activity, and stranddisplacement activity.

As used herein, the term “primer” is an oligonucleotide (“oligo”),generally with a free 3′-OH group that can be extended by a nucleic acidpolymerase. For a template-dependent polymerase, generally at least the3′-portion of the primer oligo is complementary to a portion of atemplate nucleic acid, to which the oligo “binds” (or “complexes,”“anneals,” or “hybridizes”), by hydrogen bonding and other molecularforces, to the template to give a primer/template complex for initiationof synthesis by a DNA polymerase, and which is extended by the additionof covalently bonded bases linked at its 3′-end which are complementaryto the template in the process of DNA synthesis. The result is a primerextension product.

As used herein, the term “universal sequence” refers to a region ofnucleotide sequence that is common to or shared by, two or more nucleicacid molecules. Optionally, the two or more nucleic acid molecules alsohave regions of sequence differences. Thus, for example, the 5′ tags cancomprise identical or universal nucleic acid sequences and the 3′ tagscan comprise identical or universal sequences. A universal sequence thatmay be present in different members of a plurality of nucleic acidmolecules can allow the replication or amplification of multipledifferent sequences using a single universal primer that iscomplementary to the universal sequence.

As used herein, the terms “solid surface,” “solid support” and othergrammatical equivalents herein refer to any material that is appropriatefor or can be modified to be appropriate for the attachment of apolynucleotide. Possible substrates include, but are not limited to,glass and modified or functionalized glass, plastics (includingacrylics, polystyrene and copolymers of styrene and other materials,polypropylene, polyethylene, polybutylene, polyurethanes, Teflon™,etc.), polysaccharides, nylon or nitrocellulose, ceramics, resins,silica or silica-based materials including silicon and modified silicon,carbon, metals, inorganic glasses, plastics, optical fiber bundles, anda variety of other polymers. In some embodiments, solid supports andsolid surfaces are located within a flow cell apparatus. In someembodiments, the solid support comprises a patterned surface suitablefor immobilization of transposome complexes in an ordered pattern. A“patterned surface” refers to an arrangement of different regions in oron an exposed layer of a solid support. In some embodiments, the solidsupport comprises an array of wells or depressions in a surface. Thecomposition and geometry of the solid support can vary with its use. Insome embodiments, the solid support is a planar structure such as aslide, chip, microchip and/or array. As such, the surface of a substratecan be in the form of a planar layer. In some embodiments, the solidsupport comprises one or more surfaces of a flowcell. The term“flowcell” as used herein refers to a chamber comprising a solid surfaceacross which one or more fluid reagents can be flowed. Examples offlowcells and related fluidic systems and detection platforms that canbe readily used in the methods of the present disclosure are described,for example, in Bentley et al., Nature 456:53-59 (2008), WO 04/018497;U.S. Pat. No. 7,057,026; WO 91/06678; WO 07/123744; U.S. Pat. Nos.7,329,492; 7,211,414; 7,315,019; 7,405,281, and US 2008/0108082, each ofwhich is incorporated herein by reference. In some embodiments, thesolid support or its surface is non-planar, such as the inner or outersurface of a tube or vessel. In some embodiments, the solid supportcomprises microspheres or beads. “Microspheres,” “beads,” “particles,”or grammatical equivalents herein are intended to mean small discreteparticles made of various material including, but are not limited to,plastics, ceramics, glass, and polystyrene. In certain embodiments, themicrospheres are magnetic microspheres or beads. Alternatively oradditionally, the beads may be porous. The bead sizes range fromnanometers, e.g. 100 nm, to millimeters, e.g. 1 mm.

Methods for Preparing a Library of Tagged Nucleic Acid Fragments

The present disclosure relates generally to methods for preparing alibrary of nucleic acid fragments, and more specifically to methods forpreparing a library of nucleic acid fragments in a single reactionmixture, e.g., a single reaction tube or other container, usingproteases, for a variety of applications including, e.g., nextgeneration DNA sequencing, analysis of copy number variations, andanalysis of single nucleotide variations.

There are a variety of methods and applications for which it isdesirable to prepare a library of nucleic acid fragments from a minimalpopulation of cells, e.g., a single cell, for various applications suchas sequencing a genome. Current methods for preparing a library ofnucleic acid fragments require a separate nucleic acid extraction and/oramplification step prior to DNA fragmentation. Typically, the cells areprocessed first to generate a cell lysate from which target nucleic acidcontent is extracted and purified. Then in a separate step, the purifiedtarget nucleic acid is subjected to fragmentation, e.g., using Nexteratransposome available from Illumina, Inc (San Diego, Calif.). Thisseparate nucleic acid extraction step and transfer of samples betweenreaction tubes or containers are usually wasteful of target nucleic acidsample, and thus render the nucleic acid fragments prepared less likelyto sufficiently represent across the target nucleic acid from thesample. This insufficient representation becomes particularlychallenging when the amount of cell sample is limited or difficult toobtain. Some methods have been developed to solve this problem in thecase of a single or few cell input by a pre-amplification step. However,these methods do not efficiently solve the problem of insufficientrepresentation and typically introduce high noises. The presentdisclosure provides a solution to this problem by using asingle-reaction mixture, e.g., in a single tube, with add-on protocol togenerate a library of nucleic acid fragments. The method provided hereinintegrates various steps, including generating cell lysate,tagmentation, and the like, in a single reaction tube, optionally usingone or more add-on protocols. In such a single-tube add-on method, theamount of starting nucleic acid materials from the cells are preserved,and the library generated therefrom can thus better represent the targetnucleic acid, e.g., a genome.

In one aspect, the present disclosure provides a method of preparing alibrary of tagged nucleic acid fragments including (a) contacting apopulation of cells directly with a lysis reagent to generate a celllysate, wherein the lysis reagent has one or more proteases, and whereinthe cell lysate contains a target nucleic acid; (b) inactivating the oneor more proteases to form an inactivated cell lysate, and (c) directlyapplying at least one transposase and at least one transposon endcomposition containing a transferred strand to the inactivated celllysate under conditions where the target nucleic acid and the transposonend composition undergo a transposition reaction to generate a mixture,wherein: (i) the target nucleic acid is fragmented to generate aplurality of target nucleic acid fragments, and (ii) the transferredstrand of the transposon end composition is joined to 5′ ends of each ofa plurality of the target nucleic acid fragments to generate a pluralityof 5′ tagged target nucleic acid fragments.

In some embodiments, the cell sample is directly contacted with acombined lysis reagent containing one or more proteases and thus theproteases provided herein can directly contact with the intact cells. Insome embodiments, the cell sample is contacted with a first lysisreagent containing detergents to generate a first cell lysate, and thena second lysis reagent containing one or more proteases is added to thereaction tube containing the first cell lysate. In this alternative, theproteases provided herein contact with the cell lysate. Example 1provided below illustrates a method of generating a cell lysatecontaining target nucleic acid. Exemplary lysis master mixturecontaining detergent and QIAGEN (San Diego, Calif.) protease (Part No.19155) is illustrated in Example 1 and Tables 1-3.

The starting material according the method provided herein can be aminimal population of cells, with which the traditional sequencingprotocols typically can only produce noisy sequencing data and copynumber variation data due to insufficient representatives across targetnucleic acid, e.g., a genome. In some embodiments, a minimal populationof cells can contain one, two, three, four, or five cells. In someembodiments, a minimal population of cells can be less than 10 cells,less than 15 cells, less than 20 cells, less than 25 cells, less than 30cells, less than 35 cells, less than 40 cells, less than 45 cells, lessthan 50 cells, less than 60 cells, less than 70 cells, less than 80less, less than 90 cells, or less than 100 cells. In one embodiment, thestarting material used in the present method contains only a singlecell. In some embodiments, the target nucleic acid is genomic DNA. Insome embodiments, the target nucleic acid contains chromosomal DNA or afragment thereof. In some embodiments, the target nucleic acid comprisesa genome or a partial genome.

The proteases used herein can digest chromatin proteins, e.g., histones,and other DNA binding proteins to release naked genomic DNA. Inaddition, the proteases provided herein can digest endogenous DNase toprotect the genome from degradation. In some embodiments, the methodherein uses only one protease possessing a broad specificity, and thusthe proteases can digest various different proteins and polypeptidesincluding some or many of the proteins in a cell. In some otherembodiments, the broad specificity can be achieved by using a mixture ofvarious proteases, and the combination of various proteases can digestvarious different proteins and polypeptides including some or many ofthe proteins in a cell. Exemplary proteases includes subtilisins such asALCALASE, subtilisin carlsberg, subtilisin S41, heat-labile proteinaseK, and QIAGEN protease. Example 4 illustrates that protease activity isuseful for uniform access to genomic DNA. It should be appreciated thatdifferent protease and/or mixture of proteases can be used depending onvarious conditions, e.g., cell type and sample amount.

The amount and concentration of proteases used in each reaction providedherein can vary depending on the amount of chromosome DNA and/or thenumber of the cells used as well as the activity of the proteases. Insome embodiments, the concentration of one or more proteases in the celllysate is 0.1 mg/ml to 10 mg/ml. In some embodiment, the concentrationof one or more proteases in the cell lysate is 0.1 mg/ml to 2.5 mg/ml.In some embodiments, the concentration of one or more proteases in thecell lysate is 2 mAU/ml to 500 mAU/ml. In some embodiments, theconcentration of one or more proteases in the cell lysate is 4.5 mAU/mlto 500 mAU/ml. In some embodiments, the concentration of one or moreproteases in the cell lysate is 10 mAU/ml to 100 mAU/ml. The presentdisclosure exemplifies the testing and optimizing of the proteaseconcentration using a protease, e.g., QIAGEN protease (Part No. 19155)as shown in Example 5. As shown in this example, when a single cell istreated with 0.5 mg/ml (equivalent to 22.5 mAU/ml) or 2 mg/ml(equivalent to 90 mAU/ml) protease under normal reaction temperature(e.g., room temperature), clean copy number analysis result is similarlyachieved as shown in the top two histograms of FIG. 3A. Thus, in someembodiments, the concentration of the proteases in the cell lysate is0.5 mg/ml to 2 mg/ml. Exemplary the concentrations of the proteases inthe cell lysate include 0.5 mg/ml, 0.6 mg/ml, 0.7 mg/ml, 0.8 mg/ml, 0.9mg/ml, 1.0 mg/ml, 1.1 mg/ml, 1.2 mg/ml, 1.3 mg/ml, 1.4 mg/ml, 1.5 mg/ml,1.6 mg/ml, 1.7 mg/ml, 1.8 mg/ml, 1.9 mg/ml, and 2.0 mg/ml. In someembodiments, the concentration of one or more proteases in the celllysate is 20 mAU/ml to 90 mAU/ml. Exemplary concentrations of one ormore proteases in the cell lysate include 20 mAU/ml, 30 mAU/ml, 40mAU/ml, 50 mAU/ml, 60 mAU/ml, 70 mAU/ml, 80 mAU/ml, 90 mAU/ml.

Various conditions including PH value can affect both the digestion byproteases and actives of other enzymes in the reaction tube, and thusthese conditions, e.g., pH value, can be optimized. Example 6illustrates optimizing pH condition of protease digestion reactionbalancing the protease activity and sequencing results. As shown, theQIAGEN protease activity is analyzed under different pH conditions, andthe activity of protease increases as pH value increases with proteasehaving lowest activity at pH 7.0 and highest activity at pH 10.0 amongthe range from pH 7.0 to pH 10.0. Then, percentage of unique mapped readand noise in copy number data are analyzed under various pH conditionstoo. As shown, when pH is 7, 8 or 9, about 70% clean unique mapped readscan be achieved. However, when pH is 10, less percentage of uniquemapped reads can be achieved and the data variation increasessignificantly. Similarly, when pH is 7, 8 or 9, count differencesbetween neighboring bins are relatively small (about 20%) with smallvariations; while count differences between neighboring bins aresignificantly increased with huge variation at pH 10.0. Thus, in someembodiments, the population of cells is contacted with the lysis reagentat pH7.0 to pH10.0. In some embodiments, the population of cells iscontacted with the lysis reagent at pH7.0 to pH 9.0. Exemplary pHcondition includes pH 7.0, pH 7.5, pH 8.0, pH 8.5, pH 9.0, and pH 9.5.

Because nucleic acid preparation and tagmentation steps are performed inthe same reaction tube, it can be beneficial that the proteasesaccording to the present method can be effectively inactivated withoutdisturbing the next tagmentation step which typically requiresdouble-stranded DNA. In some embodiments, the proteases can beinactivated by increasing temperature prior to the tagmentation step.High temperature can denature double-stranded DNA conformation. Thus, insome embodiments, the proteases provided herein can be inactivated atrelatively low temperature without denaturing double-stranded DNA.Example 7 illustrates testing heat inactivation of a protease. As shown,the protease activity is tested in different temperature, and theprotease activity progressively decreases as the temperature increases,and is completely inactivated at 70° C. Thus, in some embodiments, oneor more proteases are inactivated by increasing temperature to 50°C.-80° C. In some embodiments, the one or more proteases are inactivatedby increasing temperature to 70° C.

In some embodiments, the proteases provided herein can also beinactivated by adding proteases inhibitors to the reaction tube. Theprotease inhibitors provided herein do not interfere with thetagmentation and amplification step to be carried out in the samereaction tube later. Exemplary protease inhibitors include, for example,AEBSF, bestatin, E-64, pepstatin A, phosphoramidon, leupeptin,aprotinin, bestatin hydrochloride, leupeptin, phosphoramidon disodiumsalt, elastatinal, aprotinin, nafamostat mesylate, antipain, PMSF(phenylmethanesulfonylfluoride), PefaBloc, diisopropylfluorophosphate,and Streptomyces subtilisin inhibitor.

As discussed above, one or more detergents can also be added to cells.In some embodiments, the detergents are added to the cells together withthe proteases. In other embodiments, the detergents are added to thecells first followed by adding proteases to the reaction tube. Thefunction of detergent used herein includes disrupting cell membranes andreleasing intracellular materials in a soluble form. In someembodiments, the detergent used herein does not interfere withdown-stream enzymatic activities. Thus, in some embodiments, nonionicdetergents are used. These detergents break protein-lipid andlipid-lipid associations, but not protein-protein interactions, and thusare less likely to interfere other down-stream enzymes. Typically,non-ionic detergents contain uncharged, hydrophilic headgroups. Typicalnon-ionic detergents are based on polyoxyethylene or a glycoside.Exemplary non-ionic detergents include Tween® 80, Tween® 20Tween,Triton® X-100, Triton® X-100-R, Triton® X-114, NP-40, Genapol® C-100,Genapol® X-100, Igepal® CA 630, Arlasolve® 200, Brij® 96/97Triton, Brij®98, Brij® 58, Brij® 35Brij series, Pluronic® L64, Pluronic® P84,non-detergent sulfobetaines (NDSB 201), amphipols (PMAL-C8), CHAPS,octyl β-D-glucopyranoside, saponin, nonaethylene glycol monododecylether (C12E9, polidocenol), sodium dodecyl sulfate, N-laurylsarcosine,sodium deoxycholate, bile salts, hexadec yltrimethyl ammonium bromide,SB3-10, SB3-12, amidosulfobetaine-14, octyl thioglucoside, maltosides,HEGA and MEGA series.

Once the proteases are inactivated, an in vitro transposition reactioncan be carried out in the same reaction mixture, e.g., in the samereaction tube, by adding transposome composition containing a stablecomplex formed between the transposase and the transposon endcomposition or using separate transposase and transposon endcomposition. The in vitro transposition reaction catalyzed by atransposase results in simultaneously breaking a target nucleic acidinto fragments and joining a tag to the 5′ end of each fragment. Itshould be understood that any method that describes the use of atransposase and a transposon end composition could also use atransposome composition made from the transposase and the transposon endcomposition, and any method that describes the use of a transposomecomposition could also use the separate transposase and a transposon endcomposition of which the transposome composition is composed.

In some embodiments, the method provided herein includes incubating theinactivated cell lysate containing the target nucleic acid in an invitro transposition reaction with at least one transposase and atransposon end composition with which the transposase forms atransposition complex, the transposon end composition including (i) atransferred strand that exhibits a transferred transposon end sequenceand, optionally, an additional sequence 5′-of the transferred transposonend sequence, and (ii) a non-transferred strand that exhibits a sequencethat is complementary to the transferred transposon end sequence, underconditions and for sufficient time wherein multiple insertions into thetarget nucleic acid occur, each of which results in joining of a firsttag containing the transferred strand to the 5′ end of a nucleotide inthe target nucleic acid, thereby fragmenting the target nucleic acid andgenerating a population of annealed 5′-tagged DNA fragments, each ofwhich has the first tag on the 5′-end of the target nucleic acidfragments.

In some embodiments, the method described above is performed usingseparate transposase and transposon end compositions. In otherembodiments, the method described above is performed using a transposomecomposition comprising the complex formed between the transposase andthe transposon end composition.

In some specific embodiments, the method provided herein is performedusing Nextera Transposome available from the Illumina Inc (San Diego,Calif.), as described generally in the disclosure of US 2010/0120098,the content of which is incorporated herein by reference in itsentirety.

Transposases and transposome compositions are generally known to thoseof skill in the art, as exemplified by the disclosure of US2010/0120098, the content of which is incorporated herein by referencein its entirety. In some embodiments, the method provided herein employsa transposome composition formed by a hyperactive Tn5 transposase and aTn5-type transposon end (Goryshin and Reznikoff, 1998, J. Biol. Chem.,273: 7367). In some embodiments, the method provided herein employs atransposome composition formed or by a MuA transposase and a Mutransposon end comprising R1 and R2 end sequences (Mizuuchi, 1983, Cell,35: 785; Savilahti et al., 1995, EMBO J., 14: 4893). Any transpositionsystem that is capable of inserting a transposon end in a random or inan almost random manner with sufficient efficiency to 5′-tag andfragment a target nucleic acid for its intended purpose can be used inthe present disclosure. Exemplary transposome composition systemsinclude but are not limited to Staphylococcus aureus Tn552 (Colegio etal., 2001, J Bacterid., 183: 2384-8; Kirby et al., 2002, Mol Microbiol,43: 173-86), TyI (Devine and Boeke, 1994, Nucleic Acids Res., 22:3765-72 and International Patent Application No. WO 95/23875),Transposon Tn7 (Craig, 1996, Science. 271: 1512; Craig, 1996, Review in:Curr Top Microbiol Immunol, 204: 27-48), TnIO and ISIO (Kleckner et al.,1996, Curr Top Microbiol Immunol, 204: 49-82), Mariner transposase(Lampe et al., 1996, EMBO J., 15: 5470-9), Tci (Plasterk, 1996, Curr TopMicrobiol Immunol, 204: 125-43), P Element (Gloor, 2004, Methods MolBiol, 260: 97-114), TnJ (Ichikawa and Ohtsubo, 1990, J Biol Chem. 265:18829-32), bacterial insertion sequences (Ohtsubo and Sekine, 1996,Curr. Top. Microbiol. Immunol. 204:1-26), retroviruses (Brown et al.,1989, Proc Natl Acad Sci USA, 86: 2525-9), and retrotransposon of yeast(Boeke and Corces, 1989, Annu Rev Microbiol. 43: 403-34).

As non-limiting examples, transposon ends can include the 19-bp outerend (“OE”) transposon end, inner end (“IE”) transposon end, or “mosaicend” (“ME”) transposon end recognized by a wild-type or mutant Tn5transposase, or the R1 and R2 transposon end as set forth in thedisclosure of US 2010/0120098, the content of which is incorporatedherein by reference in its entirety. Transposon ends can include anynucleic acid or nucleic acid analogue suitable for forming a functionalcomplex with the transposase or integrase enzyme in an in vitrotransposition reaction. For example, the transposon end can include DNA,RNA, modified bases, non-natural bases, modified backbone, and caninclude nicks in one or both strands.

In some embodiments, wherein the transferred strand includes a3′-portion and a 5′-portion, wherein the 3′-portion exhibits transferredtransposon end sequence, and the 5′-portion of the transferred strandexhibits a sequence comprising one or more tag domains for a particularpurpose (e.g., a sequencing tag domain or an amplification tag domain,and optionally an address tag domain for next-generation sequencing oramplification). Exemplary tag domains include a restriction site tagdomain, a capture tag domain, a sequencing tag domain, an amplificationtag domain, a detection tag domain, an address tag domain, and atranscription promoter domain.

In some embodiments, two different transposomes are used in the in vitrotransposition reaction, and each of the two transposomes contains thesame transposase but a different transposon end composition. In someembodiments, two different transposomes are used, and the two differenttransposomes each contains the same transposase and the transposon endcompositions contain different transferred strands. In some embodiments,two different transposomes are used, and each of the two transposomesincludes different transposase enzymes and different transposon endcompositions, each of which forms a functional complex with therespective transposase.

In some embodiments, the amount of the transposase and the transposonend composition or of the transposome composition used in the in vitrotransposition reaction is between about 1 picomole and about 25picomoles per 50 nanograms of target nucleic acid per 50-microliterreaction. In some embodiments, the amount of the transposase and thetransposon end composition or of the transposome composition used in thein vitro transposition reaction is between about 5 picomoles and about50 picomoles per 50 nanograms of target nucleic acid per 50-microliterreaction. In some embodiments, concentration of the transposase is 0.5-1nM. In some embodiments, concentration of the transposase is 0.01-0.02picomoles per 20 μl reaction.

Example 2 illustrates a protocol for tagmentation step using a methodprovided herein. In the embodiments wherein a single-cell is used toprepare a library for sequencing, only two copies of genome are present,and thus smaller insert size tends to increase library diversity. Asshown in Example 8, the counts, and thus the diversity represented by alibrary, increase as the insert size decreases. Therefore, in someembodiments, the method herein use higher amount of transposase in thetagmentation step to increase fragmentation and reduce insert size ofthe tagged nucleic acid fragments. As shown, when 1 μl Tn5 is used in atagmentation reaction, the average fragment size is about 550 bp; whilewhen 2 μl Tn5 is used in a tagmentation reaction, the average fragmentsize is about 400 bp. Consistent with smaller insert size, librarydiversity increases when treated with 2 μl Tn5 compared with thattreated with 1 μl Tn5. Tn5 is used to illustrate adjustment oftransposase. It should be appreciated that other transposases can alsobe used in the present methods and their amount can be adjusted andoptimized using the method provided herein and methods known by thoseskilled in the art.

In some embodiments, the reaction time for the in vitro transpositionreaction is two hours or less, one hour or less, 30 minutes or less, 15minutes or less, or 10 minutes or less. In some embodiments, thereaction time for the in vitro transposition reaction is 5 minutes orless.

In some embodiments, the reaction temperature for the in vitrotransposition reaction is from about 40° C. to about 70° C., from about45° C. to about 65° C., or from about 50° C. to about 60° C. In someembodiments, the reaction temperature for the in vitro transpositionreaction is about 55° C.

In some embodiments, the in vitro transposition reaction can beterminated by holding the sample, e.g., in a tube, at 4° C. In someembodiments, neutralize tagment buffer to the tagmentation products andincubate the sample at room temperature for 5 minutes.

Through an in vitro transposition reaction, target nucleic acidfragments are tagged at the 5′ end. In some embodiments, the methodprovided herein further includes steps to incorporate a 3′ end tag tothe 5′ tagged nucleic acid fragments to make a library of di-taggednucleic acid fragments. In some embodiments, a library of di-taggednucleic acid fragments is generated from 5′ tagged target nucleic acidin a single tube without performing any intervening purification steps.Adding 3′ end tag can be performed through various methods, e.g., byusing DNA polymerase, terminal transferase, and/or ligase as describedin WO 2010/048605 the content of which is incorporated by its entirety.

Thus, in some embodiments, the method provided herein further comprises(d) incubating the mixture from step (c) directly with at least onenucleic acid modifying enzyme under conditions wherein a 3′ tag isjoined to the 5′ tagged target nucleic acid fragments to generate aplurality of di-tagged target nucleic acid fragments. In someembodiments, steps (a), (b), (c), and (d) are performed in a singlereaction tube. Embodiments illustrating generation of a library ofdi-tagged nucleic acid fragments are discussed below.

In some embodiments, di-tagged nucleic acid fragments are generated byusing a polymerase, e.g., a DNA polymerase, with strand-displacement or5′ nuclease activity. In some embodiments, the method provided hereinincludes incubating the population of annealed 5′-tagged nucleic acidfragments with a DNA polymerase that has strand-displacement or 5′nuclease activity under conditions without thermocycling and wherein theannealed 5′-tagged nucleic acid fragments are not denatured, wherein theDNA polymerase extends the 3′-end of each strand of the annealed5′-tagged nucleic acid fragments using the complementary strand as atemplate and displaces or digests the non-transferred strand, therebygenerating the library of di-tagged double-stranded DNA fragments. Inone embodiment, the extension step was performed at 72° C. using the 5′tag on the opposite strand as a template.

In some embodiments, the di-tagged double stranded DNA fragmentsgenerated by the method provided above are denatured to generate alibrary of tagged DNA fragments containing di-tagged single stranded DNAfragments (e.g., by heating to 95° C. and rapidly cooling).

In other embodiments, di-tagged nucleic acid fragments are generated byusing terminal transferase. In some embodiments, the 5′-tagged doublestranded nucleic acid fragments are denatured to generate the 5′-taggedsingle stranded nucleic acid fragments. The 5′-tagged single strandednucleic acid fragments are incubated with a DNA polymerase consisting ofa terminal transferase and at least one substrate for the terminaltransferase during which the terminal transferase joins a second tag tothe 3′ end of the 5′-tagged nucleic acid fragments, thereby generating alibrary of tagged nucleic acid fragments containing di-tagged nucleicacid fragments. In some embodiments, the 3′-end of the non-transferredtransposon end that composes the transposon end composition is blocked(e.g., by using a non-transferred transposon end that has a dideoxynucleotide or a 3′-O-methyl-nucleotide as the 3′-terminal nucleotide),which blocks 3′ nucleotide and prevents addition by terminaltransferase, thereby preventing background tagging of thenon-transferred transposon end.

In other embodiments, the 5′-tagged double stranded nucleic acidfragments are not denatured to generate the 5′-tagged single strandednucleic acid fragments. Instead, the 5′-tagged nucleic acid fragmentsare incubated, without a prior denaturation step, with a DNA polymeraseconsisting of a terminal transferase and at least one substrate for theterminal transferase under conditions and for sufficient time whereinthe terminal transferase joins the second tag to the 3′ end of the5′-tagged nucleic acid fragments, thereby generating a library ofdi-tagged nucleic acid fragments. In some embodiments, the 3′-end of thenon-transferred transposon end that composes the transposon endcomposition is blocked (e.g., by using a non-transferred transposon endthat has a dideoxy nucleotide or a 3′-O-methyl-nucleotide as the3′-terminal nucleotide).

In other embodiments, di-tagged nucleic acid fragments are generated byusing a DNA polymerase and a terminal tagging oligonucleotide. In someembodiments, the 5′-tagged double stranded nucleic acid fragments aredenatured to generate 5′-tagged single stranded nucleic acid fragments(e.g., by heating to 95° C. and rapidly cooling), and a second tag isjoined to the 3′ end of 5′-tagged single stranded nucleic acid fragmentusing a DNA polymerase and a terminal tagging oligonucleotide, therebygenerating a library of di-tagged nucleic acid fragments. In someembodiments, steps of joining the second tag to the 3′ end of the5′-tagged nucleic acid fragments using a DNA polymerase and a terminaltagging oligonucleotide includes: (1) providing a terminal taggingoligonucleotide having a 5′-portion and 3′-portion, the 5′-portionexhibits a sequence that is complementary to the sequence of the secondtag that it is desired to join to the 3′-termini of the 5′-tagged singlestranded nucleic acid fragments, and the 3′-portion exhibits a randomsequence containing between three and eight random nucleotides, ofwhich, the 3′-terminal nucleotide is blocked so that it is not capableof being extended by the DNA polymerase; (2) contacting the 5′-taggedsingle stranded nucleic acid fragments with the terminal taggingoligonucleotide under conditions and for sufficient time wherein theterminal tagging oligonucleotide anneals to the 5′-tagged singlestranded nucleic acid fragments; and (3) contacting the 5′-tagged singlestranded nucleic acid fragments to which the terminal taggingoligonucleotide is annealed with the DNA polymerase in a reactionmixture and under DNA polymerization conditions and for sufficient timewherein the 3′-termini of the 5′-tagged single stranded nucleic acidfragments are extended using the terminal tagging oligonucleotide as atemplate, whereby the second tag is joined to their 3′-termini and 5′-and 3′-tagged single stranded nucleic acid fragments are generated.

In yet other embodiments, di-tagged nucleic acid fragments are generatedby using a template-dependent ligase and a ligation taggingoligonucleotide. In some embodiments, the 5′-tagged nucleic acidfragments are incubated with a template-dependent DNA ligase and aligation tagging oligodeoxynucleotide having a 3′-portion and a5′-portion, wherein the 3′-portion exhibits a second tag that exhibitsany sequence that is desired to be joined to the 3′-end of the 5′-taggedDNA fragments and the 5′-portion has a 5′-monophosphate group andexhibits a random sequence, under conditions and for sufficient timewherein the second tag is joined to the annealed 5′-tagged DNAfragments, thereby generating a library of DNA fragments comprisingannealed di-tagged DNA fragments. In some embodiments, the methodfurther includes the step of denaturing the library of DNA fragmentscomprising annealed di-tagged DNA fragments (e.g., by heating to 95° C.and rapidly cooling), thereby generating a library of di-tagged singlestranded DNA fragments.

After a library of tagged nucleic acid fragments is generated, thetagged nucleic acid fragments can be amplified, e.g., usinglimited-cycle polymerase chain reaction (PCR), to introduce other endsequences or adaptors, e.g., index, universal primers and othersequences required for cluster formation and sequencing. In someembodiments, such amplification is performed to a library of 5′ taggednucleic acid fragments. In some embodiments, such amplification isperformed to a library of di-tagged nucleic acid fragments. In someembodiments, the amplification is performed in the same reaction tubewhere the library of tagged nucleic acid fragments is generated, and theagents for amplification are directly added to the same reaction tube.

Thus, the method provided herein further includes (e) amplifying one ormore di-tagged target nucleic acid fragments to generate a library oftagged nucleic acid fragments with additional sequence at 5′ end and/or3′ end of the di-tagged nucleic acid fragments. In some embodiments,steps (a), (b), (c), (d), and (e) are performed in a single reactiontube. Exemplary amplification methods include polymerase chain reaction(PCR), strand-displacement amplification reaction, rolling circleamplification reaction, ligase chain reaction, transcription-mediatedamplification reaction, and loop-mediated amplification reaction.

In some embodiments, the method provided herein includes amplifying thelibrary of di-tagged single stranded nucleic acid fragments using a PCR.In some embodiments, the method provided herein uses single-primer PCRamplification of a library of di-tagged DNA fragments. In someembodiments, the step of amplifying di-tagged DNA fragments includesusing a DNA polymerase and at least one primer that is complementary tothe second tag. In some embodiments, the step of amplifying the libraryof di-tagged DNA fragments includes amplifying the library of tagged DNAfragments by PCR using only one oligodeoxyribonucleotide that exhibitsthe sequence of at least a portion of the transferred strand as a PCRprimer and the di-tagged DNA fragments as templates. In someembodiments, the primer contains a 5′ portion that contains additionalsequence, e.g., an adaptor sequence.

In some embodiments, two different PCR primers are used, each of whichPCR primers exhibits the sequence of at least a portion of thetransferred transposon end that composes the transposon end composition.In some embodiments, each PCR primer includes a 3′-portion and a5′-portion, wherein the 3′-portion exhibits the respective transferredtransposon end sequence and the 5′-portion exhibits the sequence of arespective tag domain or an adaptor for a particular purpose (e.g., asequencing tag domain/adaptor or an amplification tag domain/adaptor,and optionally an address tag domain/adaptor for next-generationsequencing or amplification). For example, when a single transposon endcomposition is used in the in vitro transposition reaction to generatethe library of di-tagged DNA fragments using a DNA polymerase that hasstrand-displacement or 5′ nuclease activity, the di-tagged DNA fragmentscan be amplified by PCR using two different PCR primers. Each PCR primercontains a 3′-portion and a 5′-portion, wherein the 3′-portion exhibitsthe respective transferred transposon end sequence and the 5′-portionexhibits the sequence of a respective tag domain/adaptor for aparticular purpose (e.g., a sequencing tag domain/adaptor or anamplification tag domain/adaptor, and optionally an address tagdomain/adaptor for next-generation sequencing or amplification). In someembodiments, the 5′ portion of each PCR primer is different from that ofthe other primer, and as such the sequences of the two ends of the PCRproduct are different. For example, one end contains one index and/oruniversal primer sequence, and the other end contains a different indexand/or universal primer sequence.

In some embodiments, the two ends of di-tagged nucleic acid fragmentsoriginate from two different transferred strand sequences. For example,in some embodiments, two different transposomes can be used in the invitro transposition reaction, and each of the two transposomes containsthe same transposase but a different transposon end composition. In someembodiments, two different transposomes are used, and the two differenttransposomes each contains the same transposase and the transposon endcompositions contain different transferred strands. In some embodiments,two different transposomes are used, and each of the two transposomesincludes different transposase enzymes and different transposon endcompositions, each of which forms a functional complex with therespective transposase. In some embodiments, wherein two differenttransposon end compositions are used in the in vitro transpositionreaction, and the library of di-tagged single stranded nucleic acidfragments is generated using a DNA polymerase that hasstrand-displacement or 5′ nuclease activity, the first tag exhibits thesequence of the transferred strand of one transposon end composition andthe second tag exhibits the sequence of the non-transferred strand ofthe other transposon end composition.

In the above mentioned embodiments and other embodiments wherein twodifferent transferred strands are linked to the 5′ end of each oppositestrands of the double stranded nucleic acid, the method provided hereincan further include the step of amplifying the di-tagged nucleic acidfragments by PCR using two different PCR primers. One of the PCR primersexhibits the sequence of at least a portion of one transferred strandthat compose one transposon end composition, and the other of PCRprimers exhibits the sequence of at least a portion of the othertransferred strand that composes the other transposon end composition.

In some embodiments wherein two primers are used, each PCR primercontains a 3′-portion and a 5′-portion, wherein the 3′-portion exhibitsthe respective transferred transposon end sequence and the 5′-portionexhibits the sequence of a respective tag domain/adaptor for aparticular purpose (e.g., a sequencing tag domain or an amplificationtag domain, and optionally an address tag domain for next-generationsequencing or amplification). In some embodiments, the 5′ portion ofeach PCR primer is different from that of the other primer, and as suchto introduce different sequences to the two ends of the PCR product. Insome embodiments, the 5′ portion of the first PCR primer or the 5′portion of the second PCR primer, or the 5′ portions of both the firstand the second PCR primers contain first or second sequencingtags/adaptors, respectively, for generation of templates fornext-generation sequencing for a particular sequencing platform (e.g.,sequencing tags for an Illumina Nextera sequencing platform). In someembodiments, the 5′ portion of the first PCR primer or the 5′ portion ofthe second PCR primer additionally contains an address tagdomain/adaptor or another tag domain/adaptor for a particular purpose.

Example 3 illustrates a limited-cycle PCR amplification that can addother sequences at the two ends of the tagged nucleic acid fragments,e.g., index 1 (i7) and index 2 (i5) (from Illumina, Inc, San Diego,Calif.) and sequences required for other purposes, e.g., clusterformation. In a single-cell sequencing, the input DNA is relative small,and thus the cycle number of PCR can be adjusted to achieve bettersequencing results. In Example 9, the cycle number of PCR is tested andoptimized using a single cell as starting material. As shown, the noiseis big when PCR with 16 cycles is used in a copy number analysis, andthe noise is significantly reduced when PCR with 18 cycles or 20 cyclesis used. Thus, in some embodiments, the number of PCR cycle is 18, 19 or20.

A wide variety of enzymes and kits are available for performing theamplification reaction by PCR as known by those skilled in the art. Forexample, in some embodiments, the PCR amplification is performed usingeither the FAILSAFE™ PCR System or the MASTERAMP™ Extra-Long PCR Systemfrom EPICENTRE Biotechnologies, Madison, Wis., as described by themanufacturer. However, the present disclosure is not limited to the useof those products or conditions for the amplification reaction and anysuitable thermostable DNA polymerase and reaction mixture that permitsamplification of the sequence between the primer that anneals to thetarget sequence and the primer that anneals to the transposon can beused.

The method provide herein is not limited to the use of PCR to amplifythe library of tagged nucleic acid fragments. Any suitable amplificationmethod (e.g., rolling circle amplification, riboprimer amplification(e.g., U.S. Pat. No. 7,413,857), ICAN, UCAN, ribospia, terminal tagging(U.S. Patent Application No. 20050153333), Eberwine-type aRNAamplification or strand-displacement amplification) that amplifies thesame sequence, and generates a suitable composition and amount ofamplification product for the intended purpose can be used inembodiments of the present invention. For example, some stranddisplacement methods that can be used are described in PCT PatentPublication Nos. WO 02/16639; WO 00/56877; and AU 00/29742; of TakaraShuzo Company, Kyoto, Japan; U.S. Pat. Nos. 5,523,204; 5,536,649;5,624,825; 5,631,147; 5,648,211; 5,733,752; 5,744,311; 5,756,702; and5,916,779 of Becton Dickinson and Company; U.S. Pat. Nos. 6,238,868;6,309,833; and 6,326,173 of Nanogen/Becton Dickinson Partnership; U.S.Pat. Nos. 5,849,547; 5,874,260; and 6,218,151 of Bio Merieux; U.S. Pat.Nos. 5,786,183; 6,087,133; and 6,214,587 of Gen-Probe, Inc.; U.S. Pat.No. 6,063,604 of Wick et al; U.S. Pat. No. 6,251,639 of Kurn; U.S. Pat.No. 6,410,278; and PCT Publication No. WO 00/28082 of Eiken KagakuKabushiki Kaishi, Tokyo, Japan; U.S. Pat. Nos. 5,591,609; 5,614,389;5,773,733; 5,834,202; and 6,448,017 of Auerbach; and U.S. Pat. Nos.6,124,120; and 6,280,949 of Lizardi.

In some embodiments, the libraries of tagged nucleic acid fragmentsprepared by any method of the present disclosure can then be subject tosteps for purifying the library nucleic acid and optionally forproviding a size selection. These steps can help clean up the PCRproducts and remove nucleic acid with undesirable size. Various methodsin the art can be used to clean nucleic acid fragments generated in thepresent methods, including but not limited to, using columns to clean upthe fragments, e.g., using QIAGEN QIAQUICK PCR purification kit, andusing gel size selection, e.g., using Pippin Prep electrophoresisplatform. Other methods for cleaning up nucleic acid fragments and/orfor selecting nucleic acid size known in the art can also be used in themethod provided herein.

For example, in some embodiments, AMPURE XP beads (from Beckman CoulterGenomics) are used to purify the tagged nucleic acid fragments. Nucleicacid fragments can bind to solid-phase reversible immobilization (SPRI)beads, and the affinity of the nucleic acid fragments with differentlength to the beads can be controlled by altering the PEG/NaClconcentration. Thus, by altering the PEG/NaCl concentration, nucleicacid with different size can be selectively purified. In someembodiments, the method provided herein uses a single AMPURE XPtreatment to remove nucleic acid fragments below a certain size (e.g.,150-200 bp). In some embodiments, a double (upper and lower) sizeselection can be performed by two consecutive AMPURE XP steps. In thefirst selection step, a low concentration of AMPURE XP beads is added tothe sample to bind larger DNA fragments. In this step the beadscontaining the larger fragments are discarded. Then in the secondselection step, more beads are then added to the supernatant. In thissecond step, the amount of PEG and NaCl is increased so that smallerfragment sizes will be bound. Next the supernatant containing very shortlibrary fragments is discarded and the beads are washed and intermediatefragments are eluted. Those skilled in the art would understand thatdepending on the concentrations of PEG and NaCl in the first and finalSPRI step distinct size ranges can be generated as illustrated inBronner et al., 2009, Curr Protoc Hum Genet. 18:10.

Typical procedure for cleaning up a library of nucleic acid fragmentsusing AMPURE XP beads includes (1) vortexing AMPURE XP beads to ensurethat the beads are evenly dispersed; (2) adding certain amount of AMPUREXP beads to each PCR product generated and incubating at roomtemperature; (3) placing the tubes in a tube holder on the magneticstand until the supernatant has cleared; (5) removing and discarding thesupernatant; (6) without removing the tubes from the magnetic stand,washing the beads once or multiple times; (7) with the tubes still onthe magnetic stand, allowing the beads to air-dry; (8) removing thetubes from the magnetic stand and adding resuspension buffer andincubating at room temperature; and (9) transferring the supernatant tofresh tubes.

After the library of nucleic acid fragments are cleaned up and sizeselected, it can be further subject to a library normalization step tonormalize the quantity of each library and ensure that roughly equallibrary representation in each pooled sample. In some embodiments, abead-based library normalization process is used in the method providedherein. In a bead-based library normalization process, roughly equalamount of beads are added to each well containing a sample of nucleicacid fragments. Because the amount of the beads added in each well areroughly equal, the amount of nucleic acid fragments attached to thebeads are also roughly equal in each well. As such, after thesupernatant is removed, and nucleic acid fragments eluted from the beadscan be in roughly equal amount in each well.

A typical bead-based library normalization process includes (1) addingroughly equal amount of beads (e.g., in a bead buffer) into each wellcontaining nucleic acid fragments generated in the methods providedabove; (2) incubating and/or shaking to allow binding of the beads withnucleic acid fragments; (3) placing wells (can be on a plate) on amagnetic stand and allowing the supernatant to become cleared; (4) withwells on the magnetic stand, carefully removing and discarding thesupernatant; (5) washing beads once or multiple times; and (6) elutingthe nucleic acid fragments attached to the beads.

In some embodiments, the library of tagged nucleic acid fragmentsgenerated by the method provided herein can be used as templates fornucleic acid sequencing.

In some embodiments, prior to sequencing, the tagged nucleic acidfragments in the library are amplified to intensify signals againstnoise during a sequencing, e.g., in a sequencing by synthesis. In someembodiments, the library of tagged nucleic acid fragments is used astemplate for an amplification reaction (e.g., a PCR amplificationreaction using PCR primers that are complementary to end sequences ofthe tagged nucleic acid fragments). In some embodiments, the library ofamplified tagged nucleic acid fragments contains most or approximatelyall of the sequences exhibited by the target nucleic acid. In someembodiments wherein the target nucleic acid includes genomic DNA of anorganism, the amplification reaction is a whole genome amplificationreaction.

In some embodiments, the tagged nucleic acid fragments can beimmobilized on a solid surface. For example, the solid surface can beattached with a polynucleotide complementary to an end sequence oftagged nucleic acid fragments, and as such the tagged nucleic acidfragments can be immobilized on the solid surface. Then the immobilizednucleic acid fragments are amplified on the surface. For example, insome embodiments, the immobilized nucleic acid fragments are amplifiedusing cluster amplification methodologies as exemplified by thedisclosures of U.S. Pat. Nos. 7,985,565 and 7,115,400, the contents ofeach of which is incorporated herein by reference in its entirety. Theincorporated materials of U.S. Pat. Nos. 7,985,565 and 7,115,400describe methods of solid-phase nucleic acid amplification which allowamplification products to be immobilized on a solid support in order toform arrays comprised of clusters or “colonies” of immobilized nucleicacid molecules. Each cluster or colony on such an array is formed from aplurality of identical immobilized polynucleotide strands and aplurality of identical immobilized complementary polynucleotide strands.The arrays so-formed are generally referred to herein as “clusteredarrays.” The products of solid-phase amplification reactions such asthose described in U.S. Pat. Nos. 7,985,565 and 7,115,400 are so-called“bridged” structures formed by annealing of pairs of immobilizedpolynucleotide strands and immobilized complementary strands, bothstrands being immobilized on the solid support at the 5′ end, e.g., viaa covalent attachment. Cluster amplification methodologies are examplesof methods wherein an immobilized nucleic acid template is used toproduce immobilized amplicons. Other suitable methodologies known in theart can also be used to produce immobilized amplicons from immobilizedtagged nucleic acid fragments produced according to the methods providedherein.

The library of tagged nucleic acid fragments prepared according to themethod provided herein can be sequenced according to any suitablesequencing methodology, such as direct sequencing, including sequencingby synthesis, sequencing by ligation, sequencing by hybridization,nanopore sequencing and the like. In some embodiments, the immobilizedDNA fragments are sequenced on a solid support. In some embodiments, thesolid support for sequencing is the same solid support upon which theamplification occurs.

In some embodiments, the sequencing methodology used in the methodprovided herein is sequencing-by-synthesis (SBS). In SBS, extension of anucleic acid primer along a nucleic acid template (e.g. a target nucleicacid or amplicon thereof) is monitored to determine the sequence ofnucleotides in the template. The underlying chemical process can bepolymerization (e.g. as catalyzed by a polymerase enzyme). In aparticular polymerase-based SBS embodiment, fluorescently labelednucleotides are added to a primer (thereby extending the primer) in atemplate dependent fashion such that detection of the order and type ofnucleotides added to the primer can be used to determine the sequence ofthe template.

Other sequencing procedures that use cyclic reactions can be used, suchas pyrosequencing. Pyrosequencing detects the release of inorganicpyrophosphate (PPi) as particular nucleotides are incorporated into anascent nucleic acid strand (Ronaghi, et al., 1996, AnalyticalBiochemistry 242(1), 84-9; Ronaghi, 2001, Genome Res. 11(1), 3-11;Ronaghi et al., 1998, Science 281(5375), 363; U.S. Pat. Nos. 6,210,891;6,258,568 and 6,274,320, each of which is incorporated herein byreference). In pyrosequencing, released PPi can be detected by beingimmediately converted to adenosine triphosphate (ATP) by ATPsulfurylase, and the level of ATP generated can be detected vialuciferase-produced photons. Thus, the sequencing reaction can bemonitored via a luminescence detection system. Excitation radiationsources used for fluorescence based detection systems are not necessaryfor pyrosequencing procedures. Useful fluidic systems, detectors andprocedures that can be adapted for application of pyrosequencing toamplicons produced according to the present disclosure are described,for example, in WIPO Pat. App. Ser. No. PCT/US11/57111, US 2005/0191698A1, U.S. Pat. Nos. 7,595,883, and 7,244,559, each of which isincorporated herein by reference.

Some embodiments can utilize methods involving the real-time monitoringof DNA polymerase activity. For example, nucleotide incorporations canbe detected through fluorescence resonance energy transfer (FRET)interactions between a fluorophore-bearing polymerase andγ-phosphate-labeled nucleotides, or with zeromode waveguides (ZMWs).Techniques and reagents for FRET-based sequencing are described, forexample, in Levene et al., 2003, Science 299, 682-686; Lundquist et al.,2008, Opt. Lett. 33, 1026-1028; Korlach et al., 2008, Proc. Natl. Acad.Sci. USA 105, 1176-1181, the disclosures of which are incorporatedherein by reference.

Some SBS embodiments include detection of a proton released uponincorporation of a nucleotide into an extension product. For example,sequencing based on detection of released protons can use an electricaldetector and associated techniques that are commercially available fromIon Torrent (Guilford, Conn., a Life Technologies subsidiary) orsequencing methods and systems described in US 2009/0026082 A1; US2009/0127589 A1; US 2010/0137143 A1; or US 2010/0282617 A1, each ofwhich is incorporated herein by reference. Methods set forth herein foramplifying target nucleic acids using kinetic exclusion can be readilyapplied to substrates used for detecting protons. More specifically,methods set forth herein can be used to produce clonal populations ofamplicons that are used to detect protons.

Another useful sequencing technique is nanopore sequencing (see, forexample, Deamer et al., 2000, Trends Biotechnol., 18, 147-151; Deamer etal., 2002, Acc. Chem. Res. 35:817-825; Li et al., 2003, Nat. Mater.2:611-615), the disclosures of which are incorporated herein byreference). In some nanopore embodiments, the target nucleic acid orindividual nucleotides removed from a target nucleic acid pass through ananopore. As the nucleic acid or nucleotide passes through the nanopore,each nucleotide type can be identified by measuring fluctuations in theelectrical conductance of the pore. (U.S. Pat. No. 7,001,792; Soni etal., 2007, Clin. Chem., 53, 1996-200; Healy, 2007, Nanomed. 2, 459-481;Cockroft et al., 2008, J. Am. Chem. Soc., 130, 818-820, the disclosuresof which are incorporated herein by reference).

In some embodiments, the method provided herein further includesanalyzing copy number variation of a cell. A copy number analysis testsfor DNA copy number variation in a sample. Such analysis helps detectchromosomal copy number variation that may cause or may increase risksof various critical disorders. For example, autism has been reported tobe associated with copy number mutations (Sebat et al., 2007, Strongassociation of de novo copy number mutations with autism, Science 316(5823): 445-9). It has also been reported that schizophrenia isassociated with copy number variations (St Clair, 2008, Copy numbervariation and schizophrenia, Schizophr Bull 35 (1): 9-12). Variousmethods have been developed for detecting copy number variation.However, when starting material is limited and comes from a minimalpopulation of cells, the noise is significant and result is compromised.The present method provides a method for detecting copy number variationin such situation. Examples provided below demonstrate copy numbervariation analysis using the present methods and several parameters areoptimized for copy number variation analysis. In some embodiments, theminimal population of cells used in the copy number variation analysiscontains one, two, three, four, or five cells. Typically, as cell numberincreases, more complete read distribution can be achieved and thus lessnoise is present in the data as shown in Example 10. In this example,the read distribution using one, three or five cells in analyzed in thisexample. As shown, genomic coverage increases as the cell numberincreases, it is estimated that one cell can cover about 40% of thegenome, and three cells can cover more than 50% of genome, and fivecells can cover about 60% of the genome. The average library countsusing one cell, three cells, and five cells are about 5 million, 15million, and 20 million, respectively. Also shown in this example, whena single cell is used, the overall success rate is relatively high 94%(N=187). One cell assay failures are likely caused by quality of thecell itself, e.g., selecting one of replicating cells orapoptotic/necrotic cells.

Example 11 compares the present method with some current single cellpreparation methods. When the REPLI-g Single Cell Kit developed byQIAGEN (San Diego, Calif.) is used for preparation nucleic acid, thecopy number variation data is very noisy when derived from a singlecell, three cells or five cells. When SurePlex (PicoPlex) developed byIllumina, Inc (San Diego, Calif.) is used for preparing nucleic acid, itreduces noises compared with REPLI-g Single Cell Kit. As shown, thepresent method (Nextera SC) further reduces the noise compared withusing SurePlex Amplification System. Thus, the present method providesan advanced method for analyzing copy number variation.

One aspect of copy number variation analysis is to detect mosaicism. Amosaic or mosaicism denotes the presence of two or more genotypes in oneindividual. There are two major types of mosaicism: somatic mosaicismand germline mosaicism. Somatic mosaicism occurs when the somatic cellscontain more than one genotype, e.g., due to mitotic errors at first orlater cleavages. Researchers have shown that somatic mutations areincreasingly present throughout a lifetime and are responsible for manyleukemia, lymphomas, and solid tumors (Jacobs et al., 2012, DetectableClonal Mosaicism and Its Relationship to Aging and Cancer, NatureGenetics 44 (6): 651-U668). In germline mosaicism, some gametes (spermor oocytes) carry a mutation, but the rest are normal, which also leadsto many diseases. Thus, detection of mosaicism can provide valuablediagnostic information. The present disclosure provides methods fordetecting mosaicism. In Example 12, using the method provided herein todetect mosaicism is exemplified. As shown, a population representing15.4 MB DNA is detected in each single-cell sequencing in a copy numberanalysis of chromosome 18 of a single GM50121 cell. Similarly, copynumber analysis data of chromosomes 15, X, and 10 using a singleGM20916, and copy number analysis data of chromosomes 1 and 11 using asingle GM10239 cell both detect additional populations representingother chromosomes.

The present methods can also be used for other applications, e.g.,pre-implantation genetic screening, single cell research, analysis ofcirculating tumor cells, fine needle aspiration biopsy, buffy coat, andanalysis of amniocytes. In these applications, the nucleic acid materialto start with is usually limited, and thus the present method canimprove analysis for these applications. Besides copy number variationanalysis, the present method can also be used to detect singlenucleotide variant present in a minimal population of cells in the abovementioned applications. Single nucleotide variant includes singlenucleotide polymorphism (SNP) and point mutation. Single nucleotidepolymorphism (SNP) is a common type of genetic variation which includespolymorphism in a DNA position at which two or more alternative basesoccur at appreciable frequency in the people population (usually morethan or equal to 1%). Point mutations are base variations with thefrequency less than 1%. Single nucleotide polymorphism (SNP) and pointmutations represent the largest source of diversity in the genome of ahuman. These single nucleotide polymorphisms (SNP) and point mutationscan serve as biological markers for locating a disease on the humangenome map because they are usually located near a gene associated witha certain disease. Thus, detection of single nucleotide polymorphisms(SNPs), point mutations, and similar mutations are of great importanceto clinical activities, human health, and control of genetic disease.The present method provides advantage of uniform access to genomic DNA,and helps to preserve target nucleic acid material. Thus, it can improvesingle nucleotide variation detection using a minimal population ofcells.

In the description of some embodiments of the various methods above,“reaction tube” or “tube” is used. It should be appreciated that otherreaction mediums and/or containers can also be used in the presentmethods.

Kits for Preparing a Library of Tagged Nucleic Acid Fragments

In another aspect, the present disclosure provides a kit for preparing alibrary of tagged nucleic acid fragments comprising: (a) a lysis reagenthaving one or more proteases, and (b) a transposition reactioncomposition having at least one transposase and at least one transposonend composition containing a transferred strand.

In some embodiments, the lysis reagent provided includes only oneprotease possessing a broad specificity, and thus the proteases candigest various proteins and polypeptides. In some other embodiments, thelysis reagent provided herein includes a mixture of various proteases,and the combination of various proteases can digest various proteins andpolypeptides. Exemplary proteases provided herein include serineproteases, threonine proteases, cysteine proteases, aspartate proteases,glutamic acid proteases, and metalloproteases. Exemplary protease usedherein includes a serine protease isolated from a recombinant Bacillusstrain. Exemplary proteases used herein include subtilisin and variantsthereof, including subtilisin Carlsberg, ALCALASE, and subtilisin S41.Subtilisins and variants thereof are known to those of skill in the artand include, for example ALCALASE, ALCALASE 0.6L, ALCALASE 2.5L,ALK-enzyme, bacillopeptidase A, bacillopeptidase B, Bacillus subtilisalkaline proteinase bioprase, bioprase AL 15, bioprase APL 30,colistinase, subtilisin J, subtilisin S41, subtilisin Sendai, subtilisinGX, subtilisin E, subtilisin BL, GENENASE I, ESPERASE, MAXATASE,thermoase PC 10, protease XXVII, thermoase, SUPERASE, subtilisinCarlsberg subtilisin DY, subtilopeptidase, SP 266, SAVINASE 8.0L,SAVINASE 4.0T, KAZUSASE, protease VIII, OPTICLEAN, protin A 3L,SAVINASE, SAVINASE 16.0L, SAVINASE 32.0L EX, orientase 10B, protease S,serine endopeptidase. In particular embodiments of the methods andcompositions presented herein, a heat-labile protease such as subtilisinand heat-labile variants of subtilisin can be used, as represented bythe exemplary disclosure of Davail et al., 1994, J. Biol. Chem.,26:17448-17453, which is incorporated herein by reference in itsentirety.

In some embodiments, the lysis reagent includes one or more detergents.In some embodiments, the detergent provided herein does not interferewith down-stream enzymatic activities. Thus, in some embodiments, thelysis reagent includes nonionic detergents. Typically, non-ionicdetergents contain uncharged, hydrophilic headgroups. Typical non-ionicdetergents are based on polyoxyethylene or a glycoside. Exemplarynon-ionic detergents include Tween® 80, Tween® 20Tween, Triton® X-100,Triton® X-100-R, Triton® X-114, NP-40, Genapol® C-100, Genapol® X-100,Igepal® CA 630, Arlasolve® 200, Brij® 96/97Triton, Brij® 98, Brij® 58,Brij® 35Brij series, Pluronic® L64, Pluronic® P84, non-detergentsulfobetaines (NDSB 201), amphipols (PMAL-C8), CHAPS, octylβ-D-glucopyranoside, saponin, nonaethylene glycol monododecyl ether(C12E9, polidocenol), sodium dodecyl sulfate, N-laurylsarcosine, sodiumdeoxycholate, bile salts, hexadec yltrimethyl ammonium bromide, SB3-10,SB3-12, amidosulfobetaine-14, octyl thioglucoside, maltosides, HEGA andMEGA series. In one embodiment, the lysis reagent includes componentsprovided in Tables 1-3.

In some embodiments, the transposition composition contains at least onetransposase and at least one transposon end composition including (i) atransferred strand that has a 3′-portion that exhibits the transferredtransposon end sequence and a 5′-portion that exhibits the sequence fora tag domain for use in a next-generation sequencing or amplificationreaction, and (ii) a 5′-phosphate-containing non-transferred strand thatexhibits only the non-transferred transposon end sequence, wherein thetransposase forms a complex with the transposon end composition that isactive in an in vitro transposition reaction. In some embodiments, thekit further includes a reaction buffer that contains dimethylformamidein an amount that results in it being present in the in vitrotransposition reaction at a final concentration of 10%. In someembodiments, the tag domain includes one or more of a restriction sitedomain, a capture tag domain, a sequencing tag domain, an amplificationtag domain, a detection tag domain, and an address tag domain.

In some embodiments, the transposition reaction composition includes twoor more transposon end compositions, each of the two or more transposonend compositions includes a transferred strand that differs by at leastone nucleotide.

In some embodiments, the transposase is a Tn5 transposase. In someembodiments, the transposon end composition includes a Tn5 transposonend. In one embodiment of the kit, the transposome includes a wild-typeor hyperactive Tn5 transposase or MuA transposase that is provided at aconcentration wherein the final concentration of the transposome in thein vitro transposition reaction is at least 250 nM. In some otherembodiments, the final concentrations of wild-type or hyperactive Tn5transposome or MuA transposome is at least 500 nM.

In one embodiment, the transposase in the kit is a wild-type or mutantform of Tn5 transposase (e.g., EZ-Tn5™ transposase) at a concentrationof greater than or equal to about 5 units per microliter; about 10-20units per microliter; about 20-40 units per microliter; about 40-60units per microliter; about 60-80 units per microliter; or about 80-100units per microliter. In some embodiments, the kit provided hereinincludes components provided in Table 6.

In some embodiments, the kit additional includes a modifying enzyme. Insome embodiments, the modifying enzyme is a polymerase or a ligase. Insome embodiments, the kit includes at least one other enzyme componentselected from among: a DNA polymerase that has 5′ nuclease orstrand-displacement activity; a DNA polymerase that lacks 5′ nucleaseactivity, a template-dependent NAD ligase, and a template-independentligase. In some embodiments, the at least one other enzyme component isselected from among: FAILSAFE™ DNA polymerase mix; Taq DNA polymerase,TfI DNA polymerase, T4 DNA polymerase, E. coli DNA ligase, bacteriophageTS2126 thermostable RNA ligase, Mth Rn 1 thermostable RNA ligase, andCIRCLIGASE™ thermostable ssDNA ligase.

In some embodiments wherein the at least one enzyme in the kit is atemplate-dependent ligase (e.g., E. coli DNA ligase), a high proportionof the ligase molecules are adenylated and ATP is not provided in thekit. In some embodiments wherein the at least one enzyme in the kit is atemplate-dependent ligase (e.g., E. coli DNA ligase), the kitadditionally includes a ligation tagging oligonucleotide comprising a3′-portion and a 5′-portion, wherein the 3′-portion exhibits a sequenceof a tag domain and the 5′-portion exhibits a random sequence consistingof about three to about eight nucleotides. In some embodiments, theligation tagging oligonucleotide includes a 5′-portion that exhibits arandom sequence consisting of four nucleotides.

In some embodiments wherein the at least one enzyme in the kit is atemplate-independent ligase, selected from among bacteriophage TS2126thermostable RNA ligase, Mth Rn 1 thermostable RNA ligase, andCIRCLIGASE™ thermostable ssDNA ligase, the template-independent ligaseis provided in a highly adenylated form and ATP is not provided in thekit. In one embodiment of the kit includes EZ-Tn5™ transposase and thetemplate-independent nucleic acid ligase, the EZ-Tn5 pMEDS transposonend composition includes both an EZ-Tn5 METS transferred strand that hasa 5′-monophosphate group and an EZ-Tn5 pMENTS non-transferred strandthat has a 5′-monophosphate group.

In some embodiments, the kit further includes a reagent for anamplification reaction. In some embodiments, the reagent for theamplification reaction is a reagent for PCR. In some embodiments, thereagent for the amplification reaction includes at least one primer. Insome embodiments, the at least one primer includes a 3′ portion thatexhibits the sequence of at least a portion of the transferred strand.In some embodiments, the at least one primer includes a 5′ portion thatcontains a universal sequence.

In some embodiments, the kit includes two primers, each PCR primercontains a 3′-portion and a 5′-portion, wherein the 3′-portion exhibitsthe respective transferred transposon end sequence and the 5′-portionexhibits the sequence of a respective tag domain/adaptor for aparticular purpose (e.g., a sequencing tag domain or an amplificationtag domain, and optionally an address tag domain for next-generationsequencing or amplification). In some embodiments, the 5′ portion ofeach PCR primer is different from that of the other primer. In someembodiments, the 5′ portion of the first PCR primer or the 5′ portion ofthe second PCR primer, or the 5′ portions of both the first and thesecond PCR primers contain first or second sequencing tags/adaptors,respectively. In one embodiment, the kit provided herein includes thecomponents provided in Table 7.

In some embodiments, the kit further includes a size selection reagent.In some embodiments, the size selection reagent includes AMPURE XP beads(from Beckman Coulter Genomics). Nucleic acid fragments can bind tosolid-phase reversible immobilization (SPRI) beads. In some embodiments,the size selection reagent further includes PEG and NaCl.

In some embodiments, the kit provided herein further includes a librarynormalization reagent. In some embodiments, the library normalizationreagent includes Library Normalization Additives provided by Illumina,Inc (San Diego, Calif., Part No. 15025391) and Library NormalizationBeads provided by Illumina, Inc (Part No. 15022566). In someembodiments, the library normalization reagent further includes LibraryNormalization Wash provided by Illumina, Inc (Part No. 15022565). Insome embodiments, the library normalization reagent further includeslibrary normalization storage buffer provided by Illumina, Inc (SanDiego, Calif., Part No. 15025139).

In some embodiments, the kit further includes an apparatus having asolid surface. In some embodiments, the solid surface is attached with apopulation of oligonucleotides. In some embodiments, the apparatus is aflow cell apparatus. In some embodiments, the solid surface includes apatterned surface suitable for immobilization of molecules in an orderedpattern.

From the foregoing description, it will be apparent that variations andmodifications can be made to the invention described herein to adopt itto various usages and conditions. Such embodiments are also within thescope of the following claims.

The recitation of a listing of elements in any definition of a variableherein includes definitions of that variable as any single element orcombination (or subcombination) of listed elements. The recitation of anembodiment herein includes that embodiment as any single embodiment orin combination with any other embodiments or portions thereof.

All patents and publications mentioned in this specification are hereinincorporated by reference to the same extent as if each independentpatent and publication was specifically and individually indicated to beincorporated by reference.

The following examples are provided by way of illustration, notlimitation.

EXAMPLES Example 1 Generation of Cell Lysate Containing Target NucleicAcid

In some embodiments, during the step of generating a cell lysate, cellmembranes are disrupted by the detergent during which protein-lipid andlipid-lipid association are broken, and thereby releasing intracellularmaterials in soluble form. The major function of broad-specificityprotease is to remove DNA-binding proteins such as histones from the DNAto allow uniform access of the transposase to the DNA. In someembodiments, as illustrated in this example, the detergent and theprotease provide are in a single lysis reagent mixture. The mixture isdirectly applied to the cells for generating a cell lysate containingthe target nucleic acid. As discussed above, in some embodiments, whenheat is used to inactivate the protease, it is important that the heatdoes not denature the double-stranded nucleic acid, and to ensure thatthe tagmentation step is not interfered.

In this example, the protease can be heat inactivated at 70° C., and atthis temperature the double stranded conformation of the DNA ispreserved. A protocol for generation of a cell lysate containing targetnucleic acid is illustrated in Example 1 as follows:

(1) Adequately mixed reagents by gently inverting and flicking the tubes3-5 times, followed by a brief spin in a microcentrifuge.

(2) In a clean microcentrifuge tube, combine the components in Table 1to make the 5× lysis master mixture. The lysis master mixture can bescaled up according to the number of samples, e.g., 10% extra tocompensate for losses during pipetting can be included.

TABLE 1 Components of Lysis Mater Mixture Component of lysis matermixture Volume (μl) 5X Lysis Buffer 1.1 5X Protease Stock Solution 1.1Total 2.2

The 5× lysis buffer in the above Table 1 can be prepared according tothe following Table 2:

TABLE 2 Components of 5X Lysis Buffer Stock 5X Master Mix ComponentConcentration Concentration Volume (μl) Tris-HCl (pH 8.0) 1M 250 mM 250EDTA 0.5M  5 mM 10 TRITON X-100 10% 2.5% 250 Super Q H₂O 490 Total 1000

All reagents can be adequately mixed by gently vortexing the tubeseveral times, followed by a brief spin in a microcentrifuge. This stepcan be repeated 3-5 times. The 5× lysis buffer can be stored at roomtemperature to prevent precipitation of the detergent.

5× protease stock solution can be prepared as follows: (i) preparesingle use storage aliquots by re-suspending a protease, e.g., theQIAGEN protease, directly in the glass vial by adding 2.38 ml Super QH₂O to a final concentration of 3150 mAU/ml. Ensure the protease isadequately dissolved by gently vortexing the vial several times. Aliquotthe solution into 25 μl aliquots and immediately freeze at −80° C., and(ii) remove a single use storage aliquot from the freezer and thaw andprepare the 5× protease stock solution according to the Table 3 below:

TABLE 3 Components of 5X Protease Stock Solution 5X Master Mix ComponentStock Concentration Concentration Volume (μl) QIAGEN 3150 mAU/ml 450mAU/ml 15 Protease Super Q H₂O 90 Total 105

Accordingly, the final concentration of the 5× protease stock solutionis 450 mAU/ml.

(3) Add 2 μl of the lysis master mixture prepared above to each tubecontaining a cell, positive control genomic DNA or the negative control.Incubate the samples according to the following program in a thermalcycler: 50° C. 30 min, 70° C. 20 min, and 4° C. hold.

In some embodiments, a positive control genomic DNA is included (about30 pg) in each experiment. A positive control genomic DNA can beprepared in a two-step serial dilution from a 10 ng/μ1 stock solution asprepared in Tables 4 and 5 below:

TABLE 4 Component of Intermediate Genomic DNA Dilution IntermediateComponent Stock Concentration Concentration Volume (μl) DNA 10 ng/μl 100pg/μl 2 1X RS1 198 Total 200

Then the intermediate DNA dilution prepared according to the above tablecan be subsequently diluted according to the following Table 5:

TABLE 5 Component of Final Genomic DNA Dilution Intermediate ComponentStock Concentration Concentration Volume (μl) DNA 100 pg/μl 10 pg/μl 101X PBS 90 Total 100

3 μl of the final dilution prepared in the above table can be used asinput of a positive control genomic DNA. This corresponds to 30 pg orthe genomic equivalent of 5 cells. More or less of genomic DNA can alsobe used according to the method provided herein.

Example 2 Tagmentation of Target Nucleic Acid Directly in Cell Lysate

In some embodiments, the genomic DNA in the cell lysate, e.g., asprepared in Example 1 can be tagmented (tagged and fragmented) by theNextera transposome (available from Illumina, Inc, San Diego, Calif.).The Nextera transposome can simultaneously fragments the input DNA andadds tag/adapter sequences to the ends. The tagmentation master mixturecan be directly added to the cell lysate prepared in Example 1 withoutany prior DNA purification or amplification step. The tagmentationmaster mixture can be prepared as shown in Table 6 below and the mastermixture can be scaled up, e.g., 10% extra to compensate for lossesduring pipetting, according the number of samples.

TABLE 6 Components of Tagmentation Master Mixture Component Volume (μl)Tagmentation DNA Buffer 11 Nextera Amplicon Tagment 2.2 Mixture Super QH₂O 3.3 Total 16.5

The Tagmentation DNA Buffer and Nextera Amplicon Tagment Mixture areavailable from Illumina, Inc (San Diego, Calif.; Part No. 15027866 and15031561). The Tagmentation DNA Buffer includesTris(hydroxymethyl)aminomethane, MgCl2, and dimethylformamide. NexteraAmplicon Tagment Mixture includes transposome enzyme. 15 μl of theTagmentation Master Mixture can then be added to each cell lysate, e.g.,generated from Example 1, and incubated with the cell lysate at 55° C.for 5 min, and then at 4° C. to terminate the reaction. Then neutralizetagment buffer including SDS (available from Illumina, Inc, San Diego,Calif.) can be added to the tube and incubated at room temperature for 5minutes.

Example 3 Limited-Cycle PCR Amplification

The tagmented DNA fragments, e.g., as prepared in Example 2, can beamplified by a limited-cycle PCR program. This PCR step can also addother sequences at the two ends of the tagged nucleic acid fragments,e.g., index 1 (i7) and index 2 (i5) (available from Illumina, Inc, SanDiego, Calif.) and sequences required for other purposes, e.g., clusterformation. For example, the following components in Table 7 (availablefrom Illumina, Inc, San Diego, Calif.) can be added to the neutralizedtagmentation produced from Example 3.

TABLE 7 Components for Limited-Cycle PCR Component Volume (μl) PCRMaster 15 Mixture Index 1 5 Primer (P5 primer) Index 2 5 primer (P7primer)

The PCR master mixture in Table 7 can be prepared as in Table 8 below:

TABLE 8 Components of PCR Master Mixture Stock Master Mix VolumeComponent Concentration Concentration (μl) KAPA HiFi Fidelity Buffer 5X3.33X 999 dNTP Pool 25 mM each  1.00 mM each 59.94 KAPA HiFi DNA  1 U/μl0.033 U/μl 49.95 Polymerase Super Q H₂O 391.11 Total 1500

An exemplary PCR program is as follows: 72° C. 3 min, 98° C. 30 sec, andthen 20 cycles of 98° C. 10 seconds, 60° C. 30 seconds, and 72° C. 30seconds, and finally samples are held at 4° C.

Example 4 Protease Activity is Useful for Uniform Access to DNA

The effect of protease activity on uniform access to DNA is analyzed inthis example. In particular, 0 mg/ml, 0.1 mg/ml (4.5 mAU/ml), 0.5 mg/ml(22.5 mAU/ml), or 2.5 mg/ml (112.5 mAU/ml) proteases are used to treatwhole cells and nuclei. The percentage of unique mapped read is analyzedfor each sequencing. FIG. 1 is a histogram showing the percentage ofunique mapped read in a sequencing using 0 mg/ml, 0.1 mg/ml, 0.5 mg/ml,or 2.5 mg/ml proteases treated whole cells or nuclei. As shown, thepercentage of unique mapped read increases as the concentration ofprotease increases, and this is true using both whole cell and nuclei asstarting material. It is also noted that percentage of unique mappedread using 0.5 mg/ml protease is similar to that using 2.5 mg/ml.

The effect of protease activity on uniform access to DNA is furtheranalyzed by comparing counts and copy number analysis results amongusing bulk genomic DNA control with Nextera XT library preparation,using single cell with sufficient protease activity, and using singlecell with insufficient protease activity. FIG. 2 show histograms ofcounts and copy number analysis results using bulk DNA, single celltreated with sufficient protease activity, and single cell treated withinsufficient protease activity. As shown, when relative large amount ofgenomic DNA is used with current Nextera XT library preparation method,as show in the upper panel of FIG. 2, relative clean copy numberanalysis results can be achieved with insignificant noise. When only asingle cell is used for sequencing the noise is significant and the copynumber analysis data shows scattered distribution pattern as shown inthe lower panel of FIG. 2. Surprisingly, when the single cell is treatedwith sufficient protease (0.5 mg/ml), the copy number analysis resultsare restored to be comparable with that using bulk genomic DNA, showingclean data with insignificant noise, as shown in the middle panel ofFIG. 2. This indicates that the protease can increase the accessibilityof the genomic DNA by the transposase since DNA-binding proteins can beuniformly removed.

These results show that protease activity is useful for uniform accessto DNA in sequencing.

Example 5 Optimize Protease Concentration

In this example, the concentration of protease used in the presentmethod is analyzed. FIG. 3A shows histograms of copy number analysisresults in a single cell treated with 0.5 mg/ml active protease, 2 mg/mlactive protease, or 2 mg/ml active protease. As shown, when single cellis treated with 0.5 mg/ml or 2 mg/ml active protease, clean copy numberanalysis result is similarly achieved as shown in the top two histogramsof FIG. 3A. In contrast, when reaction is performed with proteasepre-heat inactivated at 70° C., no clean copy number result can beachieved, as shown in the bottom histogram of FIG. 3A. This result showsthat protease of both 0.5 mg/ml or 2 mg/ml concentrations are effectiveand sufficient.

The percentage of unique mapped read is also analyzed in a sequencing ofa single cell treated with 0.5 mg/ml active protease, 1 mg/ml activeprotease, 2 mg/ml active protease, or 2 mg/ml pre-heat inactivated (at70° C.) protease. FIG. 3B shows a histogram of percentage of uniquemapped read in a sequencing of a single cell treated with 0.5 mg/mlactive protease, 1 mg/ml active protease, 2 mg/ml active protease, or 2mg/ml pre-heat inactivated protease, and a control sample without cells.As shown, the percentages of unique mapped reads in sequencing using asingle cell treated with 0.5 mg/ml active protease, 1 mg/ml activeprotease, and 2 mg/ml active protease are all about 65% with smallvariation. In contrast, when protease is inactivated under 70° C., evenif higher amount of protease is used, the percentage of unique mappedread is much lower with huge variations.

In addition, the noise in copy number data is analyzed by analyzingcount differences between neighboring bin count. FIG. 3C shows ahistogram of read count differences between neighboring bins (InterQuartile Range of read count difference between neighboring bin) in asequencing of a single cell treated with 0.5 mg/ml active protease, 1mg/ml active protease, 2 mg/ml active protease, or 2 mg/ml pre-heatinactivated protease, and a control sample without cells. As shown,count differences between neighboring bin count in a sequencing using asingle cell treated with 0.5 mg/ml active protease, 1 mg/ml activeprotease, and 2 mg/ml active protease are all relatively small (about20%) with small variation. In contrast, when protease is inactivatedunder 70° C., even if higher amount of protease (2 mg/ml) is used, countdifference between neighboring bin count is much bigger with hugevariations.

Collectively, these results show that protease with concentration rangefrom 0.5 mg/ml to 2.0 mg/ml (22.5 mAU/ml to 90 mAU/ml) is sufficient andeffective in the method provided herein.

Example 6 Optimize PH Condition of Protease Digestion Reaction

In this example, the pH condition of protease digestion reaction isoptimized balancing the protease activity and sequencing results.

The protease activity is analyzed under different pH conditions. Theresult is shown in FIG. 4A. FIG. 4A is a histogram showing relativeactivity (relative to protease activity at pH 8.0) of protease under pH7.0, pH 7.5, pH 8.0, pH 8.5, pH 9.0, or pH 10.0. As shown, the activityof protease increase as pH value increases with protease having lowestactivity at pH 7.0 and highest activity at pH 10.0.

The percentage of unique mapped read is then analyzed under various pHconditions. FIG. 4B shows a histogram of percentage of unique mappedread in a sequencing of a single cell treated with protease under pH7.0, pH 8.0, pH 9.0, or pH 10.0. As shown, when pH is 7, 8 or 9, about70% clean unique mapped reads can be achieved. However, when pH is 10,less percentage of unique mapped reads can be achieved and the datavariation increases significantly.

The noise in copy number data is also analyzed by comparing countdifferences between neighboring bins. FIG. 4C shows a histogram of readcount differences between neighboring bins (Inter Quartile Range of readcount difference between neighboring bin) in a sequencing of a singlecell treated with 0.5 mg/ml protease under pH 7.0, pH 8.0, pH 9.0, or pH10.0. As shown, consistent with the unique mapped read results, countdifferences between neighboring bins are relatively small (about 20%)with small variations; while count differences between neighboring binsare significantly increased with huge variation at pH 10.0.

In some embodiments, the pH value of the digestion reaction is betweenpH 7.0 to pH 9.0.

Example 7 Test Heat Inactivation of Protease

In some embodiments, the protease provided herein can be heatinactivated. As discussed above, in prepared embodiments, the proteasecan be inactivated under relatively low temperature (e.g. 70° C.) sothat the double stranded DNA conformation can be preserved for thetagmentation reaction. In this example, the protease (from QIAGEN) isanalyzed for heat inactivation and its effect on sequencing results.

The protease was pre-heated at different temperatures, and the activityof the protease was tested. The result is shown in FIG. 5A, showing ahistogram of relative protease activity when pre-heated at roomtemperature, 50° C., 60° C., or 70° C. As shown, the protease activityprogressively decreases as the temperature increases, and is completelyinactivated at 70° C. This result is consistent with results shown inExample 5 above.

The percentage of unique mapped read in sequencing of a single cell,three cells, and 15 pg genomic DNA at various temperatures are analyzed.FIG. 5B shows a histogram of percentage of unique mapped read in asequencing of a single cell, three cells, or 15 pg genomic DNA, treatedwith 2.0 mg/ml protease at room temperature, 50° C., 60° C., or 70° C.As shown, the percentage of unique mapped read decrease as temperatureincreases. However, because relatively higher concentration of protease(2.0 mg/ml) is used in the experiment, there is more tolerance forreduced protease activity at 70° C. As such, the percentage of uniquemapped read at 70° C. is still relative high even though lower thanthose treated under lower temperatures.

The count differences between neighboring bins in sequencing of a singlecell, three cells, and 15 pg genomic DNA at various temperatures arealso analyzed. FIG. 5C shows a histogram of read count differencesbetween neighboring bins (Inter Quartile Range of read count differencebetween neighboring bin) in a sequencing of a single cell, three cells,or 15 pg genomic DNA, treated with 2 mg/ml protease at room temperature,50° C., 60° C., or 70° C. As shown, the count differences betweenneighboring bins are relatively small with small variations at lowertemperature (e.g., at room temperature and 50-60° C.); while the countdifferences between neighboring bins are significantly increased withbigger variation at 70° C.

Example 8 Diversity of Library Increases with Smaller Inert Sizes

In a single-cell sequencing, only two copies of genome are present, andthus smaller insert size tends to increase library diversity. As shownin FIG. 6A, the counts, and thus the diversity represented by a library,increase as the insert size decreases. Therefore, in some embodiments,the method herein use higher amount of transposase in the tagmentationstep to increase fragmentation and reduce insert size of the taggednucleic acid fragments. FIG. 6B shows insert size of a library treatedwith 1 μl Tn5 or 2 μl Tn5. As shown, when 1 μl Tn5 is used in atagmentation reaction, the average fragment size is about 550 bp; whilewhen 2 μl Tn5 is used in a tagmentation reaction, the average fragmentsize is about 400 bp. Consistent with smaller insert size, librarydiversity increases when treated with 2 μl Tn5 compared with thattreated with 1 μl Tn5, as shown in FIG. 6C.

Example 9 Optimize PCR Cycles

In a sequencing using a minimal population of cells, the input DNA isrelative small, and thus the cycle number of PCR can be adjusted toachieve better sequencing results. In this example, the cycle number ofPCR is tested and optimized using a single cell as starting material.FIG. 7 shows histograms of counts and copy number analysis results in asequencing of a single cell according to the method provided hereinusing PCR with 16 cycles, 18 cycles, or 20 cycles. As shown, the noiseis big when PCR with 16 cycles is used, and the noise is significantlyreduced when PCR with 18 cycles or 20 cycles is used.

Example 10 Read Distribution Using One, Three, or Five Cells

The read distribution using one, three or five cells in analyzed in thisexample. FIG. 8A shows read distribution of three single-cellsequencing. As shown, the read regions are not completed overlappedamong the three single-cell sequencing. Therefore, increase cell numberscan help with broader coverage. FIG. 8B shows read distribution ofsingle-cell sequencing, three-cell sequencing, or five-cell sequencing.As shown, genomic coverage increases as the cell number increases. FIG.8C shows histograms of average library diversity and estimated genomecoverage using a single cell, three cells or five cells. As shown, it isestimated that one cell can cover about 40% of the genome, and threecells can cover more than 50% of genome, and five cells can cover about60% of the genome. The average library counts using one cell, threecells, and five cells are about 5 million, 15 million, and 20 million,respectively.

FIG. 8D shows the overall success rate. As shown, when more than onecell is used, the overall success rate is 99% (N=81). When a single cellis used, the overall success rate is also relatively high 94% (N=187).

Example 11 Comparison of Counts and Copy Number Data Among DifferentLibrary Preparation Methods

In this example, the method provided herein is compared with somecurrent single cell preparation methods.

FIG. 9A shows copy number analysis using REPLIg Single Cell (MDA) withNexteral XT library preparation. The REPLI-g Single Cell Kit developedby QIAGEN is specially designed to amplify genomic DNA from single cells(1 to <1000 cells) or purified genomic DNA with genome coverage. TheREPLI-g Single Cell Kit developed by QIAGEN uses Multiple DisplacementAmplification (MDA) technology. See Spits et al., 2006, Whole-genomemultiple displacement amplification from single cells, Nature protocols1 (4): 1965-70. However, due to MDA introduced over-amplification bias,the copy number variation data is very noisy when derived from a singlecell, three cells or five cells, as shown in FIG. 9A.

FIG. 9B shows copy number analysis using SurePlex (PicoPlex) withNexteral XT library preparation. SurePlex Amplification System developedby Illumina, Inc (San Diego, Calif.) is a solution for the extractionand amplification of DNA from single or few single cells. As shown,SurePlex Amplification System significantly reduces noise compared withMDA.

FIG. 9C shows copy number analysis using a method (Nextera SC) providedherein. As shown, the noise is further reduced compared with usingSurePlex Amplification System.

Example 12 Detection of Mosaicism

In this example, using the method provided herein to detect mosaicism isexemplified. FIG. 10A shows copy number analysis data of chromosome 18using a single GM50121 cell. Copy number data from three single-cellsequencing are shown. A population representing 15.4 MB DNA is detectedin each single-cell sequencing. FIG. 10B shows count number data ofusing a single GM20916 cell. As shown, the arrows indicate the countsoriginated from mosaicism. FIG. 10C shows copy number analysis data ofchromosomes 15, X, and 10 using a single GM20916 cell. The copy numberdata for each chromosome analyzed detects an additional populationrepresenting another chromosome. Similarly, FIG. 10D shows copy numberanalysis data of chromosomes 1 and 11 using a single GM10239 cell. Asshown in these figures, the copy number data for each chromosomeanalyzed in FIG. 10D also detects an additional population representinganother chromosome.

A number of embodiments have been described. Nevertheless, it will beunderstood that various modifications may be made. Accordingly, otherembodiments are within the scope of the following claims.

What is claimed is:
 1. A method of preparing a library of tagged nucleicacid fragments comprising: (a) contacting a population of cellscomprising at least two cells and less than 15 cells directly with alysis reagent to generate a cell lysate, wherein the lysis reagentcomprises one or more proteases, and wherein the cell lysate contains atarget nucleic acid; (b) inactivating the one or more proteases to forman inactivated cell lysate; and (c) directly applying at least onetransposase and at least one transposon end composition containing atransferred strand to the inactivated cell lysate under conditions wherethe target nucleic acid and the transposon end composition undergo atransposition reaction to generate a mixture; wherein the target nucleicacid comprises double-stranded DNA; wherein: (i) the target nucleic acidis fragmented to generate a plurality of target nucleic acid fragments,and (ii) the transferred strand of the transposon end composition isjoined to 5′ ends of each of a plurality of the target nucleic acidfragments to generate a plurality of 5′ tagged target nucleic acidfragments; wherein the target nucleic acid remains double-stranded DNAfor the duration of (a) through (c); wherein no DNA purification oramplification occurs between (a) and (c); and wherein (a), (b), and (c)are performed in a single reaction mixture.
 2. The method of claim 1,wherein the population of cells comprises less than 10 cells.
 3. Themethod of claim 1, wherein the population of cells consists of two,three, four, or five cells.
 4. The method of claim 1, wherein the one ormore proteases comprises a serine protease, a threonine protease, acysteine protease, an aspartate protease, a glutamic acid protease, or ametalloprotease.
 5. The method of claim 4, wherein the one or moreproteases comprises a serine protease.
 6. The method of claim 1, whereinthe one or more proteases comprises a proteinase K.
 7. The method ofclaim 1, wherein the one or more proteases comprises a heat labileproteinase K.
 8. The method of claim 1, wherein the one or moreproteases comprises a subtilisin.
 9. The method of claim 1, wherein theone or more proteases comprises a heat labile subtilisin.
 10. The methodof claim 1, wherein the concentration of the one or more proteases inthe cell lysate is 4.5 mAU/ml to 500 mAU/ml.
 11. The method of claim 10,wherein, wherein the concentration of the one or more proteases in thecell lysate is 22.5 mAU/ml to 90 mAU/ml.
 12. The method of claim 10,wherein the concentration of the one or more proteases in the celllysate is about 22.5 mAU/ml.
 13. The method of claim 1, wherein thepopulation of cells are contacted with the lysis reagent at pH 7.0 to pH10.0 in (a).
 14. The method of claim 13, wherein the population of cellsare contacted with the lysis reagent at pH 7.0 to pH 9.0.
 15. The methodof claim 1, wherein the one or more proteases are inactivated byincreasing the temperature in (b).
 16. The method of claim 15, whereinthe one or more proteases are inactivated by increasing the temperatureto 50° C.-80° C.
 17. The method of claim 16, wherein the one or moreproteases are inactivated by increasing the temperature to 70° C. 18.The method of claim 1, wherein the one or more proteases are inactivatedby adding one or more inhibitors of the one or more proteases.
 19. Themethod of claim 1 wherein the lysis reagent comprises one or moredetergents.
 20. The method of claim 19, wherein the one or moredetergents are nonionic detergents.
 21. The method of claim 1, whereinthe target nucleic acid comprises genomic DNA, chromosomal DNA or afragment thereof, a genome, or a partial genome.
 22. The method of claim1, wherein the at least one transposase comprises a Tn5 transposase. 23.The method of claim 1, wherein the at least one transposon endcomposition comprises a Tn5 transposon end.
 24. The method of claim 1,wherein the transferred strand comprises tag domains containing one ormore of a restriction site domain, a capture tag domain, a sequencingtag domain, an amplification tag domain, a detection tag domain, and anaddress tag domain.